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)
- 1β3+ 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 10β25% (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 doesnβt perfectly match your resume, apply anyway.