Director, MEG Lead Hematology, Medical Evidence Generation
Bristol Myers Squibb
June 30, 2026
Remote friendly (Madison, NJ)
United States
Medical Affairs
Position Summary
Medical Evidence Generation (MEG) Lead in Oncology oversees evidence generation for the Oncology portfolio (CRCs, MAST, ISRs) to align with internal strategies and accelerate pipeline development.
Responsibilities
- Facilitate collaboration between BMS and external thought leaders in community practice and academia.
- Accountable for delivering CRCs, ISRs, and MASTs from concept/ideation through governance approval and across the study lifecycle.
- Serve as point of contact for CRCs/ISRs/MASTs within Therapeutic/Disease Area teams.
- Design and drive strategies to accelerate the clinical development pipeline using external platforms, technologies, and insights.
- Advise senior functional/therapeutic leaders on external opportunities to inform integrated evidence generation plans.
- Personally lead a limited number of high-visibility projects.
- Contribute to evolution of MEG therapeutic area strategy and value proposition.
- Location: Lawrenceville (PPK), Madison (GIR), NJ or Boudry (Switzerland).
Qualifications & Required/Preferred Skills
- MD/PhD/PharmD (or equivalent) required with extensive relevant scientific/clinical experience.
- 7+ years in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience; customer-facing desirable.
- Strategic data-generation analysis, relationship building with thought leaders and internal stakeholders.
- Global healthcare/academic systems understanding; lead in ambiguous environments.
- Strong communication/interpersonal skills; in-depth clinical trial planning/project management knowledge.
- Expected 30% global travel.
Benefits (as stated)
- Health coverage (medical, pharmacy, dental, vision); wellbeing programs; 401(k), disability, life insurance, etc.
- Paid time off (flexible time off or annual vacation/holidays depending on location).
Application instructions
- If the role doesn’t perfectly match your resume, apply anyway.
Medical Evidence Generation (MEG) Lead in Oncology oversees evidence generation for the Oncology portfolio (CRCs, MAST, ISRs) to align with internal strategies and accelerate pipeline development.
Responsibilities
- Facilitate collaboration between BMS and external thought leaders in community practice and academia.
- Accountable for delivering CRCs, ISRs, and MASTs from concept/ideation through governance approval and across the study lifecycle.
- Serve as point of contact for CRCs/ISRs/MASTs within Therapeutic/Disease Area teams.
- Design and drive strategies to accelerate the clinical development pipeline using external platforms, technologies, and insights.
- Advise senior functional/therapeutic leaders on external opportunities to inform integrated evidence generation plans.
- Personally lead a limited number of high-visibility projects.
- Contribute to evolution of MEG therapeutic area strategy and value proposition.
- Location: Lawrenceville (PPK), Madison (GIR), NJ or Boudry (Switzerland).
Qualifications & Required/Preferred Skills
- MD/PhD/PharmD (or equivalent) required with extensive relevant scientific/clinical experience.
- 7+ years in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience; customer-facing desirable.
- Strategic data-generation analysis, relationship building with thought leaders and internal stakeholders.
- Global healthcare/academic systems understanding; lead in ambiguous environments.
- Strong communication/interpersonal skills; in-depth clinical trial planning/project management knowledge.
- Expected 30% global travel.
Benefits (as stated)
- Health coverage (medical, pharmacy, dental, vision); wellbeing programs; 401(k), disability, life insurance, etc.
- Paid time off (flexible time off or annual vacation/holidays depending on location).
Application instructions
- If the role doesn’t perfectly match your resume, apply anyway.