Director, Global Clinical Physician (Immunology)
Bristol Myers Squibb
September 03, 2026
Remote friendly (Princeton, NJ)
United States
Clinical Research and Development
Position Responsibilities
Medical Monitoring:
- Serve as a key contributor to the Study Delivery Team (SDT) and Clinical Development Team (CDT), partnering with Clinical Scientists to provide medical oversight on protocol development (inclusion/exclusion criteria and safety considerations)
- Lead medical and eligibility data reviews; assess safety-related serious adverse events with Worldwide Patient Safety; oversee site interactions and safety narratives
- Uphold GCP obligations for clinical conduct and safety management; maintain required training
Clinical Development Expertise & Strategy:
- Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols (drug/asset knowledge, disease area science, regulatory targets)
- Provide medical accountability across a group of studies; lead benefit/risk analyses in a matrix team environment
- Partner with Clinical Scientists to support study delivery (site activation, enrollment, adjudication of protocol violations and deviations)
- Build and maintain relationships with principal investigators and key opinion leaders to inform emerging science, biomarker research, and clinical program design
- Maintain deep disease-area knowledge via conferences/literature; provide ongoing protocol-specific medical education to study teams and investigators
Health Authority Interactions & Publications:
- Serve as medical point of expertise in key Health Authority interactions and advisory board meetings
- Author/draft clinical content for CSRs, regulatory reports, briefing books, and submission documents (with Clinical Scientists)
Qualifications and Experience / Required Skills:
- MD required (or equivalent)
- 5+ years industry and/or clinical trials experience
- Ability to communicate clearly and lead presentations in scientific/clinical settings
- Subspecialty training in applicable therapeutic area desired
- Expertise in scientific method (statistical design, analysis, interpretation)
- Expertise in drug development process and clinical plan/protocol execution components
- Strong computer literacy; ability to navigate multiple systems; Microsoft Excel/data review essential
- Strong leadership skills; ability to lead and work effectively in teams
- Domestic and International travel may be required
Compensation / Benefits (explicit):
- Starting base range(s) listed above by location; additional incentive cash/stock may be available (eligibility-based)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), disability and life insurance, and other listed protections; Paid Time Off varies by employee type
Application instructions:
- Not included in text.
Medical Monitoring:
- Serve as a key contributor to the Study Delivery Team (SDT) and Clinical Development Team (CDT), partnering with Clinical Scientists to provide medical oversight on protocol development (inclusion/exclusion criteria and safety considerations)
- Lead medical and eligibility data reviews; assess safety-related serious adverse events with Worldwide Patient Safety; oversee site interactions and safety narratives
- Uphold GCP obligations for clinical conduct and safety management; maintain required training
Clinical Development Expertise & Strategy:
- Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols (drug/asset knowledge, disease area science, regulatory targets)
- Provide medical accountability across a group of studies; lead benefit/risk analyses in a matrix team environment
- Partner with Clinical Scientists to support study delivery (site activation, enrollment, adjudication of protocol violations and deviations)
- Build and maintain relationships with principal investigators and key opinion leaders to inform emerging science, biomarker research, and clinical program design
- Maintain deep disease-area knowledge via conferences/literature; provide ongoing protocol-specific medical education to study teams and investigators
Health Authority Interactions & Publications:
- Serve as medical point of expertise in key Health Authority interactions and advisory board meetings
- Author/draft clinical content for CSRs, regulatory reports, briefing books, and submission documents (with Clinical Scientists)
Qualifications and Experience / Required Skills:
- MD required (or equivalent)
- 5+ years industry and/or clinical trials experience
- Ability to communicate clearly and lead presentations in scientific/clinical settings
- Subspecialty training in applicable therapeutic area desired
- Expertise in scientific method (statistical design, analysis, interpretation)
- Expertise in drug development process and clinical plan/protocol execution components
- Strong computer literacy; ability to navigate multiple systems; Microsoft Excel/data review essential
- Strong leadership skills; ability to lead and work effectively in teams
- Domestic and International travel may be required
Compensation / Benefits (explicit):
- Starting base range(s) listed above by location; additional incentive cash/stock may be available (eligibility-based)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), disability and life insurance, and other listed protections; Paid Time Off varies by employee type
Application instructions:
- Not included in text.