BioSpace
Overview
The Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director, USMA Oncology, is responsible for defining compound/program medical strategies and leading select medical affairs projects within a specific compound or indication. The role oversees US Medical Affairs strategy for assigned indications/assets and may manage multiple direct reports. Responsibilities
Leads the development of the US Medical Affairs strategy and execution for select indications/projects, including evidence generation, medical information and internal education, publications, scientific exchange and external data communication, and stakeholder scientific engagement. Responsible for budgets and resources for the assigned medical affairs plan activities, in collaboration with Sr. Director. Leads medical readiness activities for market launches, including strategic partnerships with brand, HEOR, RD, FMA, MIE, and global functions to create and implement launch strategies; provide medical input into commercial and market access discussions for select indications. Provides medical leadership in interactions with external stakeholders (scientific leaders, payers, societies); leads scientific engagement activities (planning advisory boards, stakeholder interactions and peer-to-peer discussions, congress engagement) and collates insights for select indications. Responsible for scientific communications and publications; interpretation of clinical data; ensuring consistency of clinical content and statements across materials; training or communicating emerging data (internal or competitive), such as congress updates and development program highlights; budgeting and forecast accuracy. In a matrix environment, represents US interests and business needs in shaping development and lifecycle management strategy for select indications/projects. Reviews External Sponsored Research and may serve as deputy regional medical lead in Global IIS Review Committee meetings. May serve as medical lead for select company-sponsored studies; manages all medical aspects such as study document development and drives execution in collaboration with USMA Clinical Operations and cross-functional/regional stakeholders. Qualifications
Education Qualifications
(from an Accredited College Or University): An advanced doctorate degree (PharmD, Ph.D., MD, DO, or equivalent) in a medical/scientific area is required. Oncology experience required. Experience Qualifications : 10 or more years of related experience or commensurate education/experience. 4 or more years’ pharma experience at local, regional, and/or global level (preferred). Excellent knowledge of current clinical practice in Oncology/Hematology or other relevant disease area (preferred). Knowledge and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR) relating to the commercialization of oncology products (preferred). Travel
up to 20%. 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 $198,160.00 - $297,240.00 Seniority level
Director Employment type
Full-time Job function
Health Care Provider Industries
Internet News
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The Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director, USMA Oncology, is responsible for defining compound/program medical strategies and leading select medical affairs projects within a specific compound or indication. The role oversees US Medical Affairs strategy for assigned indications/assets and may manage multiple direct reports. Responsibilities
Leads the development of the US Medical Affairs strategy and execution for select indications/projects, including evidence generation, medical information and internal education, publications, scientific exchange and external data communication, and stakeholder scientific engagement. Responsible for budgets and resources for the assigned medical affairs plan activities, in collaboration with Sr. Director. Leads medical readiness activities for market launches, including strategic partnerships with brand, HEOR, RD, FMA, MIE, and global functions to create and implement launch strategies; provide medical input into commercial and market access discussions for select indications. Provides medical leadership in interactions with external stakeholders (scientific leaders, payers, societies); leads scientific engagement activities (planning advisory boards, stakeholder interactions and peer-to-peer discussions, congress engagement) and collates insights for select indications. Responsible for scientific communications and publications; interpretation of clinical data; ensuring consistency of clinical content and statements across materials; training or communicating emerging data (internal or competitive), such as congress updates and development program highlights; budgeting and forecast accuracy. In a matrix environment, represents US interests and business needs in shaping development and lifecycle management strategy for select indications/projects. Reviews External Sponsored Research and may serve as deputy regional medical lead in Global IIS Review Committee meetings. May serve as medical lead for select company-sponsored studies; manages all medical aspects such as study document development and drives execution in collaboration with USMA Clinical Operations and cross-functional/regional stakeholders. Qualifications
Education Qualifications
(from an Accredited College Or University): An advanced doctorate degree (PharmD, Ph.D., MD, DO, or equivalent) in a medical/scientific area is required. Oncology experience required. Experience Qualifications : 10 or more years of related experience or commensurate education/experience. 4 or more years’ pharma experience at local, regional, and/or global level (preferred). Excellent knowledge of current clinical practice in Oncology/Hematology or other relevant disease area (preferred). Knowledge and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR) relating to the commercialization of oncology products (preferred). Travel
up to 20%. 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 $198,160.00 - $297,240.00 Seniority level
Director Employment type
Full-time Job function
Health Care Provider Industries
Internet News
#J-18808-Ljbffr