Director, Global Medical Evidence Generation Lead, Oncology

Bristol Myers Squibb · Princeton, NJ +1 more

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Medical AffairsFull-time$207k–$251kCompany career page

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Role summary

Bristol Myers Squibb seeks a Director to lead global evidence generation strategy for oncology assets, overseeing medical affairs sponsored trials, clinical research collaborations, and investigator-sponsored studies. The role requires strategic planning, protocol development, and cross-functional leadership to generate clinical data addressing unmet patient needs.

What they're looking for

Advanced degree (MD, PhD, PharmD, MS) with extensive scientific or clinical development experience
Minimum 5 years in pharmaceutical clinical development, Medical Affairs, or related field
Deep expertise in clinical research methodologies and oncology therapeutic area
Demonstrated ability to critically analyze study design and data generation opportunities
Strong cross-functional leadership experience with external thought leaders and matrix stakeholders
Understanding of GCP, ICH guidelines, and clinical trial governance requirements
Willingness to travel globally approximately 20% of the time

What you'll be doing

Define and execute integrated evidence generation strategy aligned with product and medical affairs priorities
Lead protocol development including study design, objectives, endpoints, and statistical considerations
Manage studies from concept through governance approval and data readout
Prepare and present evidence generation proposals and results to internal governance and stakeholders
Collaborate with Clinical Operations, CROs, and external research partners to ensure quality study execution

Key requirements

Therapeutic area: Oncology

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