Global Medical Affairs Director - Oncology

Role Summary

Global Medical Affairs Director - Oncology based in Cambridge, MA or Morristown, NJ. Lead oncology medical affairs strategy and evidence generation to support assets across global and local markets, partnering with clinical development, regulatory, and commercial teams to maximize patient outcomes and scientific value.

Responsibilities

• Expert internal cross-functional leadership to advance asset development, ensure successful launches, and manage lifecycle activities.
• Lead Medical Affairs activities for oncology with emphasis on clinical evidence generation and implementation therapies.
• Build trust with global external stakeholders to advance understanding of the therapeutic area and evolve treatment landscapes for pipeline assets or marketed products.
• Co-create the IEGP strategy with Medical Evidence Generation Lead and related functions for subcutaneous formulation (CSU, RWE, HEVA, MO&E) and country teams.
• Oversee insight generation plan and input to overall medical strategy for assigned assets.
• Provide strategic input to Scientific Communications teams for evidence dissemination and medical education plans.
• Lead Integrated Patient Journey (IPJ) strategy for subcut globally with Key Markets.
• Design and oversee key medical programs to drive therapeutic value of the subcutaneous formulation and address unmet needs (MAPs, diagnostics, CSRs, etc.).
• Oversee medical tactics and clinical study budgets planning and execution to ensure prioritization and alignment with strategy.

Qualifications

• Minimum 2 years of experience in Medical Affairs, MSL, or relevant Therapeutic Area capacity.
• Deep expertise in Oncology (strongly preferred).
• Expertise in international device regulation and market implementation (strongly preferred).
• Experience in strategic medical affairs or clinical development roles including KOL engagement, evidence generation, and scientific communication at global and key market levels (preferred).
• Broad drug development experience with knowledge of regulatory, market access, and reimbursement.
• Experience managing clinical trials in a pharmaceutical environment (strongly desired).
• Specialty care product launch experience at country level (strongly preferred).
• Significant line and matrix management experience with collaboration across Research, Clinical Development, Commercial, Health Economics, Value and Access, and Product Management.

Skills

• Strategic thinking and ability to drive innovation while remaining pragmatic.
• Result orientation with capability to develop and execute strategies under ambiguity.
• People leadership with ability to provide feedback, coaching, and support.
• Stakeholder relationships and influence with collaboration and teamwork.
• Commitment to highest ethical, regulatory, and scientific standards.

Education

• Advanced degree in a scientific discipline (M.D., PhD, or PharmD).
• Fluent in English.