Director, Global Clinical Physician (Alzheimer's Disease)
Bristol Myers Squibb
August 31, 2026
Remote friendly (Princeton, NJ)
United States
Medical Affairs
Position Summary / Objective
- Serves as a primary source of medical accountability and oversight for multiple clinical trials
- Matrix management across internal and external network
- Manages Phase 1–Phase 3 studies with demonstrated decision-making capabilities
- Provides medical and scientific expertise to cross-functional colleagues
Position Responsibilities
Medical Monitoring
- Leads medical data review, including eligibility review
- Manages site interactions with Clinical Scientist for medical questions/education (including safety management)
- Assesses key safety-related serious adverse events and oversees safety narratives
- Collaborates with Clinical Scientist and provides medical strategic oversight for protocol development (inclusion/exclusion and safety considerations)
- Maintains GCP and compliance obligations and required training
Clinical Development Expertise & Strategy
- Designs and develops clinical plans and protocols to meet regulatory/disease strategy targets
- Provides oversight and medical accountability for a group of studies
- Leads benefit/risk analysis for protocols in a matrix environment
- Partners with Clinical Scientists to support study execution (site activation, enrollment status, protocol deviation adjudication)
- Builds relationships with principal investigators and cultivates thought leaders
- Maintains disease-area expertise via conferences and literature review; tracks competitive/regulatory developments
- Provides ongoing medical education to support protocol-specific training
Health Authority Interactions & Publications
- Contributes to Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician
- Authors/drafts clinical content for CSRs, regulatory reports, briefing books, and submission documents
Qualifications
- MD required (or x-US equivalent)
- 5+ years industry and/or clinical trials experience required
- Subspecialty training in applicable therapeutic area desired
Key Competencies / Skills
- Clear communication and ability to lead presentations
- Scientific method expertise (statistical design, analysis, interpretation)
- Expertise in drug development process and clinical plan/protocol execution
- Strong leadership and teamwork
Travel
- Domestic and international travel may be required
- Serves as a primary source of medical accountability and oversight for multiple clinical trials
- Matrix management across internal and external network
- Manages Phase 1–Phase 3 studies with demonstrated decision-making capabilities
- Provides medical and scientific expertise to cross-functional colleagues
Position Responsibilities
Medical Monitoring
- Leads medical data review, including eligibility review
- Manages site interactions with Clinical Scientist for medical questions/education (including safety management)
- Assesses key safety-related serious adverse events and oversees safety narratives
- Collaborates with Clinical Scientist and provides medical strategic oversight for protocol development (inclusion/exclusion and safety considerations)
- Maintains GCP and compliance obligations and required training
Clinical Development Expertise & Strategy
- Designs and develops clinical plans and protocols to meet regulatory/disease strategy targets
- Provides oversight and medical accountability for a group of studies
- Leads benefit/risk analysis for protocols in a matrix environment
- Partners with Clinical Scientists to support study execution (site activation, enrollment status, protocol deviation adjudication)
- Builds relationships with principal investigators and cultivates thought leaders
- Maintains disease-area expertise via conferences and literature review; tracks competitive/regulatory developments
- Provides ongoing medical education to support protocol-specific training
Health Authority Interactions & Publications
- Contributes to Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician
- Authors/drafts clinical content for CSRs, regulatory reports, briefing books, and submission documents
Qualifications
- MD required (or x-US equivalent)
- 5+ years industry and/or clinical trials experience required
- Subspecialty training in applicable therapeutic area desired
Key Competencies / Skills
- Clear communication and ability to lead presentations
- Scientific method expertise (statistical design, analysis, interpretation)
- Expertise in drug development process and clinical plan/protocol execution
- Strong leadership and teamwork
Travel
- Domestic and international travel may be required