Director, Global Clinical Physician (Alzheimer's Disease)
Bristol Myers Squibb
August 31, 2026
Remote friendly (Princeton, NJ)
United States
Clinical Research and Development
Position Summary / Objective
- Primary source of medical accountability and oversight for multiple clinical trials
- Matrix management across internal/external network
- Manages Phase 1–Phase 3 studies; demonstrated decision-making
- Provides medical/scientific expertise to cross-functional colleagues
Position Responsibilities
Medical Monitoring
- Key member of Study Delivery Team (SDT) / Clinical Development Team (CDT)
- Lead medical data review (including eligibility review)
- Partner with Clinical Scientist (CS) for site interactions, medical questions, education, and safety management
- Assess key safety-related serious adverse events; oversee safety narratives
- Collaborate with CS on protocols (inclusion/exclusion and safety-related considerations)
- Fulfill GCP/compliance obligations and maintain required training
Clinical Development Expertise & Strategy
- Design/develop clinical plans and protocols with strategic focus to meet regulatory/disease targets
- Provide oversight/medical accountability for a group of studies
- Lead benefit/risk analysis for protocols
- Partner with CS for study delivery (site activation, enrollment status, adjudication for deviations)
- Build relationships with principal investigators and thought leaders; maintain disease-area scientific expertise
- Provide ongoing medical education with CS
Health Authority Interactions & Publications
- Medical point of expertise for Health Authority interactions/advisory boards
- Draft/author clinical content for CSRs, regulatory reports, briefing books, and submission documents
Degree Requirements
- MD required (or x-US equivalent)
Experience Requirements
- 5+ years industry and/or clinical trials experience
Key Competency Requirements
- Clear scientific/clinical communication and presentation; leadership in teams
- Subspecialty training desired
- Expertise in scientific method (stat design/analysis/interpretation) and drug development process
Travel
- Domestic and international travel may be required.
Compensation/Benefits (if applicable)
- Compensation ranges and eligibility for discretionary incentives/stock; comprehensive benefits including medical/dental/vision/life/disability, FTO (exempt U.S.), vacation/holidays (non-exempt/RayzeBio/PR), and additional time-off depending on eligibility.
Application Instructions
- U.S.-based job seekers can explore benefits at https://careers.bms.com/benefits
- Primary source of medical accountability and oversight for multiple clinical trials
- Matrix management across internal/external network
- Manages Phase 1–Phase 3 studies; demonstrated decision-making
- Provides medical/scientific expertise to cross-functional colleagues
Position Responsibilities
Medical Monitoring
- Key member of Study Delivery Team (SDT) / Clinical Development Team (CDT)
- Lead medical data review (including eligibility review)
- Partner with Clinical Scientist (CS) for site interactions, medical questions, education, and safety management
- Assess key safety-related serious adverse events; oversee safety narratives
- Collaborate with CS on protocols (inclusion/exclusion and safety-related considerations)
- Fulfill GCP/compliance obligations and maintain required training
Clinical Development Expertise & Strategy
- Design/develop clinical plans and protocols with strategic focus to meet regulatory/disease targets
- Provide oversight/medical accountability for a group of studies
- Lead benefit/risk analysis for protocols
- Partner with CS for study delivery (site activation, enrollment status, adjudication for deviations)
- Build relationships with principal investigators and thought leaders; maintain disease-area scientific expertise
- Provide ongoing medical education with CS
Health Authority Interactions & Publications
- Medical point of expertise for Health Authority interactions/advisory boards
- Draft/author clinical content for CSRs, regulatory reports, briefing books, and submission documents
Degree Requirements
- MD required (or x-US equivalent)
Experience Requirements
- 5+ years industry and/or clinical trials experience
Key Competency Requirements
- Clear scientific/clinical communication and presentation; leadership in teams
- Subspecialty training desired
- Expertise in scientific method (stat design/analysis/interpretation) and drug development process
Travel
- Domestic and international travel may be required.
Compensation/Benefits (if applicable)
- Compensation ranges and eligibility for discretionary incentives/stock; comprehensive benefits including medical/dental/vision/life/disability, FTO (exempt U.S.), vacation/holidays (non-exempt/RayzeBio/PR), and additional time-off depending on eligibility.
Application Instructions
- U.S.-based job seekers can explore benefits at https://careers.bms.com/benefits