US-MO-Kansas CityCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227018
Dec 14, 2018
US-MO-Kansas CityCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227018
US-MO-St. LouisCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227016
Dec 14, 2018
US-MO-St. LouisCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227016
US-DC | US-MD-BaltimoreCategory Medical Science LiaisonOverviewProgram: Clinical Education LiaisonsDepartment: ImmunoscienceReports To: CEL Field Manager (NFM) Location: Field Territory:DC, MD, WV, N. VA (north of Richmond) Title: Clinical Education Liaison (CEL)The Clinical Education Liaison will represent client and its approved rheumatology product.The CEL will be aligned with the client field medical function, working closely with the client field commercial and Medical teams, and responsible for interacting with a targeted and CEL identified list of external HCPs in a defined territory. The CEL will be primarily responsible for conducting presentations to HCPs (in 1:1 or group settings) of approved efficacy and safety information. In addition, the field medical staff will respond to scientific exchange in specifically defined disease and investigational compounds or research areas if applicable.ResponsibilitiesDuties and ResponsibilitiesConducts presentations of approved efficacy and safety information to HCPs (in 1:1 or group settings) identified and prioritized in collaboration with client commercial field force.Accurately responds to on-label and off-label medical questions from HCPs in accordance with approved client guidance for the CELs, and applicable laws, regulations and ethical standards and by using approved contentParticipates in required therapeutic training and demonstrates competency in communicating information on disease area and mechanism of actionAble to retain and relay information from key publications.Documents all interactions and activities in appropriate databases, retaining and submitting required expenses and meeting defined qualitative and quantitative objectives.Possesses an understanding of the pharmaceutical and healthcare industryAdheres to and manages travel and expenses to meet client and BESTMSLs policiesComplies with all approved client and BESTMSLs guidance, policies, and rules governing the implementation of the CEL role including but not limited to interactions with HCPS, client field teams (medical and commercial), and handling customers' unsolicited medical requests for on and/or off-label informationInternal and External Contacts/CustomersExternalRheumatology HCPsInternalMedical/ Field Medical (disease and Brand Leads, Field Medical Management)Commercial (Territory Business Managers (TBMs) District Business Managers (DBMs) Regional Business Directors (RBDs)MarketingLegal and ComplianceQualificationsQualificationsPharmD, PhD, or MD preferredRPh, RNs, NPs, PAs with Rheumatology clinical and field medical experience may be considered.Ideal candidate would have a minimum of two years pharmaceutical industry work experience following degree completion.Ideal candidate to demonstrate business acumen and both Rheumatology and pharmaceutical experience.Ability to quickly and comprehensively learn about new subject areas and environments.Ability to take and follow direction from leadershipWorking knowledge of and ability to perform consistent with regulatory and compliance requirementsExceptional organizational and time management skillsStrong interpersonal skills including excellent verbal and written communicationAbility to travel, locally and regionally, up to 70%.Valid driver's license.Self starter, Ability to work independently and to integrate/work in cross functional networks/matrixPhysical DemandsThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.PI106227020
Dec 14, 2018
US-DC | US-MD-BaltimoreCategory Medical Science LiaisonOverviewProgram: Clinical Education LiaisonsDepartment: ImmunoscienceReports To: CEL Field Manager (NFM) Location: Field Territory:DC, MD, WV, N. VA (north of Richmond) Title: Clinical Education Liaison (CEL)The Clinical Education Liaison will represent client and its approved rheumatology product.The CEL will be aligned with the client field medical function, working closely with the client field commercial and Medical teams, and responsible for interacting with a targeted and CEL identified list of external HCPs in a defined territory. The CEL will be primarily responsible for conducting presentations to HCPs (in 1:1 or group settings) of approved efficacy and safety information. In addition, the field medical staff will respond to scientific exchange in specifically defined disease and investigational compounds or research areas if applicable.ResponsibilitiesDuties and ResponsibilitiesConducts presentations of approved efficacy and safety information to HCPs (in 1:1 or group settings) identified and prioritized in collaboration with client commercial field force.Accurately responds to on-label and off-label medical questions from HCPs in accordance with approved client guidance for the CELs, and applicable laws, regulations and ethical standards and by using approved contentParticipates in required therapeutic training and demonstrates competency in communicating information on disease area and mechanism of actionAble to retain and relay information from key publications.Documents all interactions and activities in appropriate databases, retaining and submitting required expenses and meeting defined qualitative and quantitative objectives.Possesses an understanding of the pharmaceutical and healthcare industryAdheres to and manages travel and expenses to meet client and BESTMSLs policiesComplies with all approved client and BESTMSLs guidance, policies, and rules governing the implementation of the CEL role including but not limited to interactions with HCPS, client field teams (medical and commercial), and handling customers' unsolicited medical requests for on and/or off-label informationInternal and External Contacts/CustomersExternalRheumatology HCPsInternalMedical/ Field Medical (disease and Brand Leads, Field Medical Management)Commercial (Territory Business Managers (TBMs) District Business Managers (DBMs) Regional Business Directors (RBDs)MarketingLegal and ComplianceQualificationsQualificationsPharmD, PhD, or MD preferredRPh, RNs, NPs, PAs with Rheumatology clinical and field medical experience may be considered.Ideal candidate would have a minimum of two years pharmaceutical industry work experience following degree completion.Ideal candidate to demonstrate business acumen and both Rheumatology and pharmaceutical experience.Ability to quickly and comprehensively learn about new subject areas and environments.Ability to take and follow direction from leadershipWorking knowledge of and ability to perform consistent with regulatory and compliance requirementsExceptional organizational and time management skillsStrong interpersonal skills including excellent verbal and written communicationAbility to travel, locally and regionally, up to 70%.Valid driver's license.Self starter, Ability to work independently and to integrate/work in cross functional networks/matrixPhysical DemandsThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.PI106227020
US-OH-Cleveland | US-MI-DetroitCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227024
Dec 14, 2018
US-OH-Cleveland | US-MI-DetroitCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227024
US-TX-HoustonCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227048
Dec 14, 2018
US-TX-HoustonCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227048
US-TX-DallasCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227046
Dec 14, 2018
US-TX-DallasCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227046
US-NC-CharlotteCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227044
Dec 14, 2018
US-NC-CharlotteCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227044
US-GA-AtlantaCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227041
Dec 14, 2018
US-GA-AtlantaCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227041
US-IL-ChicagoCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227039
Dec 14, 2018
US-IL-ChicagoCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227039
US-WA-SeattleCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227037
Dec 14, 2018
US-WA-SeattleCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227037
US-MA-BostonCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227033
Dec 14, 2018
US-MA-BostonCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227033
US-CA-San FranciscoCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227035
Dec 14, 2018
US-CA-San FranciscoCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227035
US-FL-OrlandoCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227031
Dec 14, 2018
US-FL-OrlandoCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227031
US-FL-MiamiCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227029
Dec 14, 2018
US-FL-MiamiCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106227029
US-CA-San FranciscoCategory Clinical Trial LiaisonOverviewThe Clinical Trial Liaison (CTL) is a field based medical expert primarily responsible for increasing awareness of client clinical trial activities among potential referral sites and driving patient recruitment. The CTL implements these objectives through the fostering and maintaining of bi-directional scientific communication, engaging with external scientific and medical leaders and delivering scientific and medical information to support activities and strategy regarding development activities.The CTL will act as a conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesTo engage potential referral sites with the objective of driving patient enrollment. This will be done through an awareness campaign focused on the trial objectives and patient criteria. The CTL will provide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and relevant clinical staff.To identify, regularly engage and build relationships with key trial site personnelTo identify barriers to enrollment at the site and to work with the CRO, Sponsor, and Site to resolve through escalation of site issues to appropriate CRO and/or Sponsor contactsBe flexible to the demands of the role as they continuously evolveTo execute individual strategic direction and goals based on a strategic plan supported by Medical Affairs and aligned with client company goalsAct in accordance with applicable client values, including compliance, legal, GCP, other regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with Key Opinion Leaders (KOLs) with initial focus being on trial sites and referral sites.Collaborate and align with cross-functional teams such as clinical developmentAssist client Clinical Development department with company sponsored clinical trials; such as trial site identification, protocol education, as well as other requests carried out in close consultation with clinical.Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, KOL/HCP development, therapeutic options and product trainingAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Attend assigned medical and scientific meetings as deemed appropriate by Head of Medical Affairs to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Design, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to client as requestedInput regular field activity into the customer relationship management tool (Client's Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Client valuesPerform additional duties as requested by internal managementFlexibility and goal-oriented personality are essentialManage Relationships With:Medical Affairs manager/director as assigned by Head of Medical AffairsInternal: working relationships with Clinical, Compliance, Legal, Commercial teamsExternal: medical practices, research centers, national, regional and local external experts, key medical and academic centers, and therapeutic area disease and patient societies QualificationsEducation and Experience:Advanced degree preferred (PharmD, MD, DO, PhD, RN, NP or PA), with strong medical/clinical backgroundBackground in Cardiology preferred1-3 years of experience in the biopharmaceutical field; MSL, CTL (or similar role) experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trials preferredExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceWell versed in GCPs and PhRMA regulationsSkills and Attributes:Experience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (≥70%) via air, train or car sometimes in excess of 2 hoursAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesMust be fluent in English. Ability to speak French is a plus.PI106227054
Dec 14, 2018
US-CA-San FranciscoCategory Clinical Trial LiaisonOverviewThe Clinical Trial Liaison (CTL) is a field based medical expert primarily responsible for increasing awareness of client clinical trial activities among potential referral sites and driving patient recruitment. The CTL implements these objectives through the fostering and maintaining of bi-directional scientific communication, engaging with external scientific and medical leaders and delivering scientific and medical information to support activities and strategy regarding development activities.The CTL will act as a conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesTo engage potential referral sites with the objective of driving patient enrollment. This will be done through an awareness campaign focused on the trial objectives and patient criteria. The CTL will provide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and relevant clinical staff.To identify, regularly engage and build relationships with key trial site personnelTo identify barriers to enrollment at the site and to work with the CRO, Sponsor, and Site to resolve through escalation of site issues to appropriate CRO and/or Sponsor contactsBe flexible to the demands of the role as they continuously evolveTo execute individual strategic direction and goals based on a strategic plan supported by Medical Affairs and aligned with client company goalsAct in accordance with applicable client values, including compliance, legal, GCP, other regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with Key Opinion Leaders (KOLs) with initial focus being on trial sites and referral sites.Collaborate and align with cross-functional teams such as clinical developmentAssist client Clinical Development department with company sponsored clinical trials; such as trial site identification, protocol education, as well as other requests carried out in close consultation with clinical.Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, KOL/HCP development, therapeutic options and product trainingAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Attend assigned medical and scientific meetings as deemed appropriate by Head of Medical Affairs to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Design, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to client as requestedInput regular field activity into the customer relationship management tool (Client's Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Client valuesPerform additional duties as requested by internal managementFlexibility and goal-oriented personality are essentialManage Relationships With:Medical Affairs manager/director as assigned by Head of Medical AffairsInternal: working relationships with Clinical, Compliance, Legal, Commercial teamsExternal: medical practices, research centers, national, regional and local external experts, key medical and academic centers, and therapeutic area disease and patient societies QualificationsEducation and Experience:Advanced degree preferred (PharmD, MD, DO, PhD, RN, NP or PA), with strong medical/clinical backgroundBackground in Cardiology preferred1-3 years of experience in the biopharmaceutical field; MSL, CTL (or similar role) experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trials preferredExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceWell versed in GCPs and PhRMA regulationsSkills and Attributes:Experience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (≥70%) via air, train or car sometimes in excess of 2 hoursAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesMust be fluent in English. Ability to speak French is a plus.PI106227054
US-WA-SeattleCategory Clinical Trial LiaisonOverviewThe Clinical Trial Liaison (CTL) is a field based medical expert primarily responsible for increasing awareness of client clinical trial activities among potential referral sites and driving patient recruitment. The CTL implements these objectives through the fostering and maintaining of bi-directional scientific communication, engaging with external scientific and medical leaders and delivering scientific and medical information to support activities and strategy regarding development activities.The CTL will act as a conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesTo engage potential referral sites with the objective of driving patient enrollment. This will be done through an awareness campaign focused on the trial objectives and patient criteria. The CTL will provide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and relevant clinical staff.To identify, regularly engage and build relationships with key trial site personnelTo identify barriers to enrollment at the site and to work with the CRO, Sponsor, and Site to resolve through escalation of site issues to appropriate CRO and/or Sponsor contactsBe flexible to the demands of the role as they continuously evolveTo execute individual strategic direction and goals based on a strategic plan supported by Medical Affairs and aligned with client company goalsAct in accordance with applicable client values, including compliance, legal, GCP, other regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with Key Opinion Leaders (KOLs) with initial focus being on trial sites and referral sites.Collaborate and align with cross-functional teams such as clinical developmentAssist client Clinical Development department with company sponsored clinical trials; such as trial site identification, protocol education, as well as other requests carried out in close consultation with clinical.Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, KOL/HCP development, therapeutic options and product trainingAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Attend assigned medical and scientific meetings as deemed appropriate by Head of Medical Affairs to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Design, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to client as requestedInput regular field activity into the customer relationship management tool (Client's Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Client valuesPerform additional duties as requested by internal managementFlexibility and goal-oriented personality are essentialManage Relationships With:Medical Affairs manager/director as assigned by Head of Medical AffairsInternal: working relationships with Clinical, Compliance, Legal, Commercial teamsExternal: medical practices, research centers, national, regional and local external experts, key medical and academic centers, and therapeutic area disease and patient societies QualificationsEducation and Experience:Advanced degree preferred (PharmD, MD, DO, PhD, RN, NP or PA), with strong medical/clinical backgroundBackground in Cardiology preferred1-3 years of experience in the biopharmaceutical field; MSL, CTL (or similar role) experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trials preferredExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceWell versed in GCPs and PhRMA regulationsSkills and Attributes:Experience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (≥70%) via air, train or car sometimes in excess of 2 hoursAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesMust be fluent in English. Ability to speak French is a plus.PI106227052
Dec 14, 2018
US-WA-SeattleCategory Clinical Trial LiaisonOverviewThe Clinical Trial Liaison (CTL) is a field based medical expert primarily responsible for increasing awareness of client clinical trial activities among potential referral sites and driving patient recruitment. The CTL implements these objectives through the fostering and maintaining of bi-directional scientific communication, engaging with external scientific and medical leaders and delivering scientific and medical information to support activities and strategy regarding development activities.The CTL will act as a conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesTo engage potential referral sites with the objective of driving patient enrollment. This will be done through an awareness campaign focused on the trial objectives and patient criteria. The CTL will provide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and relevant clinical staff.To identify, regularly engage and build relationships with key trial site personnelTo identify barriers to enrollment at the site and to work with the CRO, Sponsor, and Site to resolve through escalation of site issues to appropriate CRO and/or Sponsor contactsBe flexible to the demands of the role as they continuously evolveTo execute individual strategic direction and goals based on a strategic plan supported by Medical Affairs and aligned with client company goalsAct in accordance with applicable client values, including compliance, legal, GCP, other regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with Key Opinion Leaders (KOLs) with initial focus being on trial sites and referral sites.Collaborate and align with cross-functional teams such as clinical developmentAssist client Clinical Development department with company sponsored clinical trials; such as trial site identification, protocol education, as well as other requests carried out in close consultation with clinical.Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, KOL/HCP development, therapeutic options and product trainingAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Attend assigned medical and scientific meetings as deemed appropriate by Head of Medical Affairs to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Design, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to client as requestedInput regular field activity into the customer relationship management tool (Client's Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Client valuesPerform additional duties as requested by internal managementFlexibility and goal-oriented personality are essentialManage Relationships With:Medical Affairs manager/director as assigned by Head of Medical AffairsInternal: working relationships with Clinical, Compliance, Legal, Commercial teamsExternal: medical practices, research centers, national, regional and local external experts, key medical and academic centers, and therapeutic area disease and patient societies QualificationsEducation and Experience:Advanced degree preferred (PharmD, MD, DO, PhD, RN, NP or PA), with strong medical/clinical backgroundBackground in Cardiology preferred1-3 years of experience in the biopharmaceutical field; MSL, CTL (or similar role) experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trials preferredExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceWell versed in GCPs and PhRMA regulationsSkills and Attributes:Experience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (≥70%) via air, train or car sometimes in excess of 2 hoursAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesMust be fluent in English. Ability to speak French is a plus.PI106227052
US-NV-Las VegasCategory Clinical Trial LiaisonOverviewThe Clinical Trial Liaison (CTL) is a field based medical expert primarily responsible for increasing awareness of client clinical trial activities among potential referral sites and driving patient recruitment. The CTL implements these objectives through the fostering and maintaining of bi-directional scientific communication, engaging with external scientific and medical leaders and delivering scientific and medical information to support activities and strategy regarding development activities.The CTL will act as a conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesTo engage potential referral sites with the objective of driving patient enrollment. This will be done through an awareness campaign focused on the trial objectives and patient criteria. The CTL will provide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and relevant clinical staff.To identify, regularly engage and build relationships with key trial site personnelTo identify barriers to enrollment at the site and to work with the CRO, Sponsor, and Site to resolve through escalation of site issues to appropriate CRO and/or Sponsor contactsBe flexible to the demands of the role as they continuously evolveTo execute individual strategic direction and goals based on a strategic plan supported by Medical Affairs and aligned with client company goalsAct in accordance with applicable client values, including compliance, legal, GCP, other regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with Key Opinion Leaders (KOLs) with initial focus being on trial sites and referral sites.Collaborate and align with cross-functional teams such as clinical developmentAssist client Clinical Development department with company sponsored clinical trials; such as trial site identification, protocol education, as well as other requests carried out in close consultation with clinical.Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, KOL/HCP development, therapeutic options and product trainingAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Attend assigned medical and scientific meetings as deemed appropriate by Head of Medical Affairs to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Design, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to client as requestedInput regular field activity into the customer relationship management tool (Client's Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Client valuesPerform additional duties as requested by internal managementFlexibility and goal-oriented personality are essentialManage Relationships With:Medical Affairs manager/director as assigned by Head of Medical AffairsInternal: working relationships with Clinical, Compliance, Legal, Commercial teamsExternal: medical practices, research centers, national, regional and local external experts, key medical and academic centers, and therapeutic area disease and patient societies QualificationsEducation and Experience:Advanced degree preferred (PharmD, MD, DO, PhD, RN, NP or PA), with strong medical/clinical backgroundBackground in Cardiology preferred1-3 years of experience in the biopharmaceutical field; MSL, CTL (or similar role) experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trials preferredExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceWell versed in GCPs and PhRMA regulationsSkills and Attributes:Experience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (≥70%) via air, train or car sometimes in excess of 2 hoursAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesMust be fluent in English. Ability to speak French is a plus.PI106227050
Dec 14, 2018
US-NV-Las VegasCategory Clinical Trial LiaisonOverviewThe Clinical Trial Liaison (CTL) is a field based medical expert primarily responsible for increasing awareness of client clinical trial activities among potential referral sites and driving patient recruitment. The CTL implements these objectives through the fostering and maintaining of bi-directional scientific communication, engaging with external scientific and medical leaders and delivering scientific and medical information to support activities and strategy regarding development activities.The CTL will act as a conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesTo engage potential referral sites with the objective of driving patient enrollment. This will be done through an awareness campaign focused on the trial objectives and patient criteria. The CTL will provide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and relevant clinical staff.To identify, regularly engage and build relationships with key trial site personnelTo identify barriers to enrollment at the site and to work with the CRO, Sponsor, and Site to resolve through escalation of site issues to appropriate CRO and/or Sponsor contactsBe flexible to the demands of the role as they continuously evolveTo execute individual strategic direction and goals based on a strategic plan supported by Medical Affairs and aligned with client company goalsAct in accordance with applicable client values, including compliance, legal, GCP, other regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with Key Opinion Leaders (KOLs) with initial focus being on trial sites and referral sites.Collaborate and align with cross-functional teams such as clinical developmentAssist client Clinical Development department with company sponsored clinical trials; such as trial site identification, protocol education, as well as other requests carried out in close consultation with clinical.Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, KOL/HCP development, therapeutic options and product trainingAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Attend assigned medical and scientific meetings as deemed appropriate by Head of Medical Affairs to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Design, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to client as requestedInput regular field activity into the customer relationship management tool (Client's Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Client valuesPerform additional duties as requested by internal managementFlexibility and goal-oriented personality are essentialManage Relationships With:Medical Affairs manager/director as assigned by Head of Medical AffairsInternal: working relationships with Clinical, Compliance, Legal, Commercial teamsExternal: medical practices, research centers, national, regional and local external experts, key medical and academic centers, and therapeutic area disease and patient societies QualificationsEducation and Experience:Advanced degree preferred (PharmD, MD, DO, PhD, RN, NP or PA), with strong medical/clinical backgroundBackground in Cardiology preferred1-3 years of experience in the biopharmaceutical field; MSL, CTL (or similar role) experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trials preferredExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceWell versed in GCPs and PhRMA regulationsSkills and Attributes:Experience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (≥70%) via air, train or car sometimes in excess of 2 hoursAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesMust be fluent in English. Ability to speak French is a plus.PI106227050
US-MO-Kansas CityCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106032103
Dec 06, 2018
US-MO-Kansas CityCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106032103
US-MO-St. LouisCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106032101
Dec 06, 2018
US-MO-St. LouisCategory Medical Science LiaisonOverviewThe Medical Science Liaison (MSL) is a field based medical expert responsible for: fostering and maintaining bi-directional scientific communication with multiple external entities, including external scientific and medical leaders, disease and patient societies, etc., and creating and updating scientific and medical information to support activities and strategy regarding products and development activities.The MSL will act as the conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines. ResponsibilitiesProvide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on Alzheimer's Disease, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and their clinical trial staffTo conduct oneself in a non-promotional manner, respond appropriately to unsolicited inquires, facilitate research oriented requests (both company sponsored and investigator initiated requests)To execute individual strategic direction and goals, as directed by the line managers based on a strategic plan supported by Medical Affairs and aligned with company goalsAct in accordance with applicable values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with External Experts (EE, or Key Opinion Leaders-KOL)Provide collaboration and alignment with cross-functional teams such as clinical development and marketing departmentsAssist Clinical Development department with company sponsored clinical trials; such as clinical trial site identification, site initiation, site protocol education, as well as other requestsRespond to unsolicited ad hoc field based requests (including MIRs-Medical Information Requests; and IRB-Institutional Review Board requests)Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, EE/HCP development, therapeutic options and product trainingCoordinate Educational ProgramsAssist in the coordination and development of medically relevant, non-CME continuing education programs (internal and external)Medical / Scientific ExchangeAttend assigned medical and scientific meetings (congresses) and symposia to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Develop and deliver presentations (e.g. formulary) using approved materialsDesign, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to the BU / company as requestedAdministrative DutiesInput regular field activity into the customer relationship management tool (Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisManage Relationships With:Accountable (reports) to manager: Manager, Regional Medical Director, or Medical Director); member of Medical Affairs departmentInternal: working relationships with R&D (Clinical Development, IIS, Innovation, Technical and manufacturing teams), Compliance, Legal, Commercial, Marketing, Market Access and Business Development teamsExternal - National, regional and local external experts, key medical and academic centers, research centers, and therapeutic area disease and patient societiesEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company valuesPerform additional duties as requested by internal management QualificationsEducation and Experience Advanced degree preferred (PharmD, MD, DO, or PhD), with strong medical/clinical backgroundBackground in Neurology and Alzheimer's Disease preferredAt least 1-3 years of experience in the biopharmaceutical and/or device field; Medical Science experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trialsExperience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceSkills and AttributesExperience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (50-70%) via air, train or car sometimes in excess of 2 hours in lengthAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesPI106032101
US-DC | US-MD-BaltimoreCategory Medical Science LiaisonOverviewProgram: Clinical Education LiaisonsDepartment: ImmunoscienceReports To: CEL Field Manager (NFM) Location: Field Territory:DC, MD, WV, N. VA (north of Richmond) Title: Clinical Education Liaison (CEL)The Clinical Education Liaison will represent client and its approved rheumatology product.The CEL will be aligned with the client field medical function, working closely with the client field commercial and Medical teams, and responsible for interacting with a targeted and CEL identified list of external HCPs in a defined territory. The CEL will be primarily responsible for conducting presentations to HCPs (in 1:1 or group settings) of approved efficacy and safety information. In addition, the field medical staff will respond to scientific exchange in specifically defined disease and investigational compounds or research areas if applicable.ResponsibilitiesDuties and ResponsibilitiesConducts presentations of approved efficacy and safety information to HCPs (in 1:1 or group settings) identified and prioritized in collaboration with client commercial field force.Accurately responds to on-label and off-label medical questions from HCPs in accordance with approved client guidance for the CELs, and applicable laws, regulations and ethical standards and by using approved contentParticipates in required therapeutic training and demonstrates competency in communicating information on disease area and mechanism of actionAble to retain and relay information from key publications.Documents all interactions and activities in appropriate databases, retaining and submitting required expenses and meeting defined qualitative and quantitative objectives.Possesses an understanding of the pharmaceutical and healthcare industryAdheres to and manages travel and expenses to meet client and BESTMSLs policiesComplies with all approved client and BESTMSLs guidance, policies, and rules governing the implementation of the CEL role including but not limited to interactions with HCPS, client field teams (medical and commercial), and handling customers' unsolicited medical requests for on and/or off-label informationInternal and External Contacts/CustomersExternalRheumatology HCPsInternalMedical/ Field Medical (disease and Brand Leads, Field Medical Management)Commercial (Territory Business Managers (TBMs) District Business Managers (DBMs) Regional Business Directors (RBDs)MarketingLegal and ComplianceQualificationsQualificationsPharmD, PhD, or MD preferredRPh, RNs, NPs, PAs with Rheumatology clinical and field medical experience may be considered.Ideal candidate would have a minimum of two years pharmaceutical industry work experience following degree completion.Ideal candidate to demonstrate business acumen and both Rheumatology and pharmaceutical experience.Ability to quickly and comprehensively learn about new subject areas and environments.Ability to take and follow direction from leadershipWorking knowledge of and ability to perform consistent with regulatory and compliance requirementsExceptional organizational and time management skillsStrong interpersonal skills including excellent verbal and written communicationAbility to travel, locally and regionally, up to 70%.Valid driver's license.Self starter, Ability to work independently and to integrate/work in cross functional networks/matrixPhysical DemandsThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.PI105950601
Dec 02, 2018
US-DC | US-MD-BaltimoreCategory Medical Science LiaisonOverviewProgram: Clinical Education LiaisonsDepartment: ImmunoscienceReports To: CEL Field Manager (NFM) Location: Field Territory:DC, MD, WV, N. VA (north of Richmond) Title: Clinical Education Liaison (CEL)The Clinical Education Liaison will represent client and its approved rheumatology product.The CEL will be aligned with the client field medical function, working closely with the client field commercial and Medical teams, and responsible for interacting with a targeted and CEL identified list of external HCPs in a defined territory. The CEL will be primarily responsible for conducting presentations to HCPs (in 1:1 or group settings) of approved efficacy and safety information. In addition, the field medical staff will respond to scientific exchange in specifically defined disease and investigational compounds or research areas if applicable.ResponsibilitiesDuties and ResponsibilitiesConducts presentations of approved efficacy and safety information to HCPs (in 1:1 or group settings) identified and prioritized in collaboration with client commercial field force.Accurately responds to on-label and off-label medical questions from HCPs in accordance with approved client guidance for the CELs, and applicable laws, regulations and ethical standards and by using approved contentParticipates in required therapeutic training and demonstrates competency in communicating information on disease area and mechanism of actionAble to retain and relay information from key publications.Documents all interactions and activities in appropriate databases, retaining and submitting required expenses and meeting defined qualitative and quantitative objectives.Possesses an understanding of the pharmaceutical and healthcare industryAdheres to and manages travel and expenses to meet client and BESTMSLs policiesComplies with all approved client and BESTMSLs guidance, policies, and rules governing the implementation of the CEL role including but not limited to interactions with HCPS, client field teams (medical and commercial), and handling customers' unsolicited medical requests for on and/or off-label informationInternal and External Contacts/CustomersExternalRheumatology HCPsInternalMedical/ Field Medical (disease and Brand Leads, Field Medical Management)Commercial (Territory Business Managers (TBMs) District Business Managers (DBMs) Regional Business Directors (RBDs)MarketingLegal and ComplianceQualificationsQualificationsPharmD, PhD, or MD preferredRPh, RNs, NPs, PAs with Rheumatology clinical and field medical experience may be considered.Ideal candidate would have a minimum of two years pharmaceutical industry work experience following degree completion.Ideal candidate to demonstrate business acumen and both Rheumatology and pharmaceutical experience.Ability to quickly and comprehensively learn about new subject areas and environments.Ability to take and follow direction from leadershipWorking knowledge of and ability to perform consistent with regulatory and compliance requirementsExceptional organizational and time management skillsStrong interpersonal skills including excellent verbal and written communicationAbility to travel, locally and regionally, up to 70%.Valid driver's license.Self starter, Ability to work independently and to integrate/work in cross functional networks/matrixPhysical DemandsThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.PI105950601