Director, Global Clinical Physician
Bristol Myers Squibb
6 days ago
Remote friendly (Lawrence, 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 with demonstrated decision-making
- Provides medical and scientific expertise to cross-functional BMS colleagues
Position Responsibilities
Medical Monitoring
- Key member of Study Delivery Team (SDT) and may be on Clinical Development Team (CDT)
- Leads medical data review (including eligibility review)
- Partners with Clinical Scientist (CS) for site interactions (medical questions/education, safety management)
- Assesses key safety-related serious adverse events with Worldwide Patient Safety; oversees safety narratives
- Collaborates with CS on protocols (inclusion/exclusion and safety-related clinical considerations)
- Fulfills GCP/compliance obligations and maintains required training
Clinical Development Expertise & Strategy
- Designs/develops clinical plans and protocols to meet regulatory and 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 CS for study execution (site activation, enrollment status, adjudication of protocol violations/deviations)
- Builds relationships with principal investigators/thought leaders; maintains disease-area medical/scientific reputation
- Provides ongoing medical education
Health Authority Interactions & Publications
- Medical point of expertise for Health Authority interactions/advisory boards
- Authors/drafts CSRs, regulatory reports, briefing books, and submission documents
Degree/Experience/Skills
- MD required (or x-US equivalent)
- 5+ years industry and/or clinical trials experience required
- Clear scientific/clinical communication; subspecialty training desired
- Expertise in scientific method/statistics; drug development process; clinical plan/protocol execution
- Strong leadership and teamwork
Travel Required
- Domestic and international travel may be required.
Benefits (high level)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), disability and life insurance; paid time off varies by location/role.
- Primary source of medical accountability and oversight for multiple clinical trials
- Matrix management across internal/external network
- Manages Phase 1–Phase 3 studies with demonstrated decision-making
- Provides medical and scientific expertise to cross-functional BMS colleagues
Position Responsibilities
Medical Monitoring
- Key member of Study Delivery Team (SDT) and may be on Clinical Development Team (CDT)
- Leads medical data review (including eligibility review)
- Partners with Clinical Scientist (CS) for site interactions (medical questions/education, safety management)
- Assesses key safety-related serious adverse events with Worldwide Patient Safety; oversees safety narratives
- Collaborates with CS on protocols (inclusion/exclusion and safety-related clinical considerations)
- Fulfills GCP/compliance obligations and maintains required training
Clinical Development Expertise & Strategy
- Designs/develops clinical plans and protocols to meet regulatory and 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 CS for study execution (site activation, enrollment status, adjudication of protocol violations/deviations)
- Builds relationships with principal investigators/thought leaders; maintains disease-area medical/scientific reputation
- Provides ongoing medical education
Health Authority Interactions & Publications
- Medical point of expertise for Health Authority interactions/advisory boards
- Authors/drafts CSRs, regulatory reports, briefing books, and submission documents
Degree/Experience/Skills
- MD required (or x-US equivalent)
- 5+ years industry and/or clinical trials experience required
- Clear scientific/clinical communication; subspecialty training desired
- Expertise in scientific method/statistics; drug development process; clinical plan/protocol execution
- Strong leadership and teamwork
Travel Required
- Domestic and international travel may be required.
Benefits (high level)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), disability and life insurance; paid time off varies by location/role.