Senior Director, US Oncology Medical Affairs, Diagnostics
Daiichi Sankyo, Trenton, New Jersey, United States
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to be an innovative global healthcare company contributing to the sustainable development of society, we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary Medical Affairs Diagnostic lead, under leadership of the Executive Director of Research and Strategy, US Oncology Medical Affairs. Develops and implements the USMA diagnostic strategy and tactical plan for all therapeutic areas as part of the US Brand Strategic Plan and leads the execution of the activities in the USMA plan including Launch Readiness and Life Cycle Management.
Responsibilities
Develops the US Medical Affairs strategy and medical objectives for all compounds and leads development and execution of the US Medical Affairs plan and budget management, including activities related to evidence generation, scientific engagement, and communication as part of Launch Readiness activities and lifecycle management from a medical perspective.
Participates in Global Medical Affairs committees as requested and in processes as US Medical Affairs Lead to gain strategic and planning alignment across the matrix team the core USMA functions.
Represents US medical affairs function as a member of cross-functional forums including Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US Product Team to inform clinical development, commercialization, market access, and other cross-functional strategic discussions.
Provides medical leadership:
Leads USMA teams as part of evidence generation forums and study teams for local/regional Medical Affairs company sponsored study concepts as needed. Partners with RWE and HEOR strategy and Biomarker/CDx leads on related integrated evidence generation strategies and activities as part of the USMA Plan.
Collaborates with Global Medical Affairs and across USMA functions to develop, review, and align on key scientific communications and medical information response documents within legal and compliance regulations. Leads internal stakeholder medical education activities related to the compound data. In partnership with Medical Intelligence and Congress Planning leads, communicates and educates on related competitor data.
Provides medical leadership in scientific engagement activities with external stakeholders such as advisory boards, investigator interactions, congress activities, and peer-to-peer discussions with key thought leaders. Supports scientific symposiums and medical congresses within legal and compliance regulations.
Works with Patient Advocacy leads and Grants office to incorporate patient voice and define external medical education strategies for independent grants.
Provides input into publication strategy, data gap analysis, and tactical planning as part of the overall USMA plan. Reviews and approves abstracts, manuscripts, and other data disclosure documents. Manages budgets and resources for USOMA-supported activities within the USMA plan, in collaboration with US Oncology Franchise Head.
Qualifications Education Qualifications Advanced scientific degree (Ph.D., PharmD or MD), equivalent will be considered with relevant experience in a health sciences related field or an equivalent combination of education and experience required. Bachelor's Degree required.
Experience Qualifications
10 or more years pharmaceutical industry experience or commensurate healthcare or research experience required.
4 or more years post-doctoral and/or relevant industry experience, and expertise in oncology biomarker and/or companion diagnostic development required.
4 or more years (in-house) medical affairs or related experience, US preferred required.
Must have oncology experience, specifically in solid tumors.
Previous overall responsibility and accountability for multiple indications of one or more compounds and related USOMA plan/budget for related MA activities.
Demonstrated ability to lead and influence others internally and externally and experience leading matrix medical teams and representing medical on cross-functional leadership teams (e.g. US Product Team, US Brand Team, Global Medical Team).
Relationships with or proven history developing key external experts.
Proven ability to manage multiple priorities at one time.
Strong knowledge of medical strategy, clinical diagnostic development, and Field Medical activities required.
Knowledge of ADC or other biologics, or small molecules.
Demonstrated experience working with an alliance partner company preferred.
Travel Requirements Ability to travel up to 20% of the time.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$230,175.00 - USD$383,625.00
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Job Summary Medical Affairs Diagnostic lead, under leadership of the Executive Director of Research and Strategy, US Oncology Medical Affairs. Develops and implements the USMA diagnostic strategy and tactical plan for all therapeutic areas as part of the US Brand Strategic Plan and leads the execution of the activities in the USMA plan including Launch Readiness and Life Cycle Management.
Responsibilities
Develops the US Medical Affairs strategy and medical objectives for all compounds and leads development and execution of the US Medical Affairs plan and budget management, including activities related to evidence generation, scientific engagement, and communication as part of Launch Readiness activities and lifecycle management from a medical perspective.
Participates in Global Medical Affairs committees as requested and in processes as US Medical Affairs Lead to gain strategic and planning alignment across the matrix team the core USMA functions.
Represents US medical affairs function as a member of cross-functional forums including Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US Product Team to inform clinical development, commercialization, market access, and other cross-functional strategic discussions.
Provides medical leadership:
Leads USMA teams as part of evidence generation forums and study teams for local/regional Medical Affairs company sponsored study concepts as needed. Partners with RWE and HEOR strategy and Biomarker/CDx leads on related integrated evidence generation strategies and activities as part of the USMA Plan.
Collaborates with Global Medical Affairs and across USMA functions to develop, review, and align on key scientific communications and medical information response documents within legal and compliance regulations. Leads internal stakeholder medical education activities related to the compound data. In partnership with Medical Intelligence and Congress Planning leads, communicates and educates on related competitor data.
Provides medical leadership in scientific engagement activities with external stakeholders such as advisory boards, investigator interactions, congress activities, and peer-to-peer discussions with key thought leaders. Supports scientific symposiums and medical congresses within legal and compliance regulations.
Works with Patient Advocacy leads and Grants office to incorporate patient voice and define external medical education strategies for independent grants.
Provides input into publication strategy, data gap analysis, and tactical planning as part of the overall USMA plan. Reviews and approves abstracts, manuscripts, and other data disclosure documents. Manages budgets and resources for USOMA-supported activities within the USMA plan, in collaboration with US Oncology Franchise Head.
Qualifications Education Qualifications Advanced scientific degree (Ph.D., PharmD or MD), equivalent will be considered with relevant experience in a health sciences related field or an equivalent combination of education and experience required. Bachelor's Degree required.
Experience Qualifications
10 or more years pharmaceutical industry experience or commensurate healthcare or research experience required.
4 or more years post-doctoral and/or relevant industry experience, and expertise in oncology biomarker and/or companion diagnostic development required.
4 or more years (in-house) medical affairs or related experience, US preferred required.
Must have oncology experience, specifically in solid tumors.
Previous overall responsibility and accountability for multiple indications of one or more compounds and related USOMA plan/budget for related MA activities.
Demonstrated ability to lead and influence others internally and externally and experience leading matrix medical teams and representing medical on cross-functional leadership teams (e.g. US Product Team, US Brand Team, Global Medical Team).
Relationships with or proven history developing key external experts.
Proven ability to manage multiple priorities at one time.
Strong knowledge of medical strategy, clinical diagnostic development, and Field Medical activities required.
Knowledge of ADC or other biologics, or small molecules.
Demonstrated experience working with an alliance partner company preferred.
Travel Requirements Ability to travel up to 20% of the time.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$230,175.00 - USD$383,625.00
[Link available when viewing the job]
#J-18808-Ljbffr