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Senior Manager, US Medical Promotional Review, Oncology

Bristol Myers Squibb
June 24, 2026
Remote friendly (Princeton, NJ)
United States
Medical Affairs
Position Summary
Senior Manager, US Medical Promotional Review (Oncology) in Medical Communications (Global Medical Affairs). Ensures medical accuracy/scientific validity and compliance for promotional and non-promotional materials within an Oncology brand/disease area.

Key Responsibilities
- Maintain therapeutic area/product knowledge via literature, guidelines, internal resources, and data assessment.
- Provide medical guidance in interdisciplinary meetings and initiatives (promotional review, disease/brand/launch planning, labeling changes, business reviews).
- Conduct Promotional Review (PReP) Advisor reviews for scientific/medical validity and adherence to BMS SOPs.
- Critically evaluate/promote strategically sound solutions for complex promotional/non-promotional tactics to ensure balanced messaging, key clinical findings, medical accuracy, and guideline support (e.g., clinical guidelines, FDA/OPDP).
- Align with marketing, access, medical, corporate communications, training, legal, and commercial regulatory affairs to coordinate messaging.
- Lead within the medical review team; drive best practices, monitor regulatory changes, support Commercial strategy, and participate in process improvements.
- Review evidence for promotional claims (comprehensive, balanced, unbiased, statistically reliable) and advise on scientific interpretation.
- Use digital/AI solutions to improve efficiency/consistency/scalability; stay current on industry trends and share best practices.
- Complete assigned SOPs/training; conduct business per BMS Values.

Qualifications & Experience
- Advanced scientific degree (PharmD, PhD, or MD preferred).
- 1–3 years clinical practice or direct pharmaceutical/healthcare Promotional Review experience (therapeutic area preferred).
- Medical writing and promotional material review knowledge.
- Ability to manage multiple projects, problem-solve, and work cross-functionally.
- Strong medical/scientific written & verbal communication; pharmaceutical compliance/conflict-of-interest knowledge.
- Ability to analyze/interpret trial data; experience with FDAMA 114, Real World Evidence, and data consistent with FDA labeling (CFL).
- Travel 10–25%.

Benefits (explicitly listed)
- Health Coverage (medical, pharmacy, dental, vision); Wellbeing programs; Financial well-being/protection (401(k), disability, life insurance, etc.).
- Paid Time Off (flexible time off or annual vacation/holidays per location/role).

Application Instructions
If the role doesn’t perfectly match your resume, apply anyway.