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Senior Manager, US Medical Promotional Review Scientist, Immunology

Bristol Myers Squibb
19 days ago
Remote friendly (Princeton, NJ)
United States
Medical Affairs
Position Summary
The Senior Manager, US Medical Promotional Review Scientist (Immunology) in Medical Communications (Global Medical Affairs) ensures medical accuracy and scientific validity of promotional and non-promotional materials within an Immunology brand/disease area, including compliance with US laws and regulations.

Key Responsibilities
- Maintain therapeutic area/product knowledge via assessment of Immunology literature, guidelines, internal resources, and data
- Provide medical guidance in interdisciplinary meetings (promotional review, disease/brand/launch planning, labeling changes, business reviews)
- As a PReP Advisor team member, review promotional/proactive materials for scientific/medical validity and adherence to BMS SOPs
- Evaluate promotional evidence and provide strategically sound solutions ensuring message balance, medical accuracy, appropriate support, and guideline-consistent content (e.g., FDA/OPDP)
- Partner cross-functionally (marketing, access, medical, training, legal, commercial regulatory affairs) to coordinate messaging
- Lead medical review best practices, regulation currency, and process improvement initiatives
- Stay current via internal/external meetings (training, education, congresses, matrix meetings)
- Review/evaluate evidence supporting promotional claims (comprehensive, balanced, unbiased, statistically reliable)
- Apply digital/AI solutions to improve efficiency, consistency, scalability
- Complete assigned SOPs/training and conduct business aligned with BMS Values

Qualifications & Experience (Required/Preferred)
- Advanced scientific degree (PharmD/PhD/MD preferred)
- 1–3+ years clinical practice or pharma/healthcare industry experience in Promotional Review (therapeutic area experience preferred)
- Knowledge of medical writing and promotional material review
- Ability to manage multiple projects; solve problems; work in multidisciplinary teams
- Strong scientific/medical written & verbal communication
- Understanding of pharma compliance/transparency/conflict-of-interest environments
- Ability to analyze/interpret trial data; experience with FDAMA 114, RWE, and FDA-approved labeling data
- Ability to travel 10–25% (domestically/internationally)

Benefits (explicitly stated)
- Health, wellbeing programs, financial protection (including 401(k), disability, life insurance)
- Paid Time Off (flexible time off and national holidays; plus additional eligible time-off)

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