Director, Strategic Evidence and Collaborations, US Medical Affairs
Core
Co-develop US Medical Affairs strategy for oncology congress plans and evidence generation across tumor types, collaborating with internal teams and external organizations like NCI/CTEP.
Role type
Director, Strategic Evidence and Collaborations (Oncology)
Builds
US and Global Medical Affairs Strategic Plans, Integrated Strategic Plan (ISP), Plan of Action (POA), and evidence generation strategies for ADC portfolio.
Domain
Biopharmaceuticals, Oncology, Medical Affairs
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Advanced medical/scientific degree (Ph.D., MD, Pharm D), 8+ years in Medical Affairs, deep subject matter expertise in ADC portfolio, strategic planning, stakeholder management, scientific data presentation, regulatory compliance knowledge.
Preferred skills
10+ years in Medical Affairs, oncology-specific experience, ability to translate strategy into actionable plans, abstract and manuscript development, knowledge of FDA regulations and ICH guidelines.
Technologies
None explicitly stated
Responsibilities
Establish and execute overarching strategy for evidence generation across tumor types, collaborate with cooperative groups and NCI/CTEP, contribute to Global Integrated Strategic Plan and Local Plan of Action, develop strategies for education and data generation, present scientific data at internal and external meetings, support US medical efforts in global congress planning, lead medical efforts for US-based Oncology Societies, serve as information resource for US Medical Science Liaisons, collaborate on Investigator Sponsored Research, review study proposals and manuscripts, support Disease-Specific Publication Strategy.
Seniority
Director, strategic leadership with hands-on execution
