Director, Medical Affairs Strategy
$230,000–$260,000 year
RemoteCambridge, Massachusetts, United States
Job Summary
Develop and execute annual Medical Affairs strategic and tactical plans while collaborating cross-functionally with Clinical, Commercial, Regulatory, and Field Medical teams to ensure alignment with scientific and business objectives. Operationalize Medical Affairs activities including advisory boards, symposia, scientific congress planning, and educational initiatives, and serve as a key contributor on the Promotional Review Committee and Medical Review Committee to ensure scientific accuracy and compliance. Support the Investigator-Sponsored Research program by reviewing proposals, coordinating internal evaluations, and communicating with investigators, while partnering with Clinical Development to integrate healthcare provider insights for clinical trial design. Collaborate with Commercial colleagues on promotional material development and assist in maintaining internal processes, SOPs, and guidance documents. Gather and synthesize scientific insights from key opinion leader interactions and conferences, manage vendor oversight and budgets, and facilitate cross-functional planning for oncology-focused initiatives.
Required Qualifications
- Advanced, medical/scientific doctoral-level degree required: PharmD, PhD, MD (or equivalent)
- 10 + years of experience in the pharmaceutical biotech or other relevant industries
- 3+ years in Medical Affairs
- Oncology experience
- Prior experience supporting advisory boards, PRC/MRC, and ISR programs
- Experience collaborating across Clinical and Commercial functions
- Strong project management and scientific communication skills
- Up to 25% domestic (and possibly international) travel
Desired Qualifications
- 3+ years in Medical Affairs is preferred
- Solid tumor experience strongly preferred
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