Sr. Clinical Trial Physician, Neuroscience
Bristol Myers Squibb
Full-time
Remote friendly (San Diego, CA)
United States
Clinical Research and Development
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Role Summary
Sr. Clinical Trial Physician, Neuroscience at Bristol Myers Squibb. Primary medical accountability and oversight for multiple clinical trials within Clinical Development, guiding design, execution, and interpretation of studies across Phases 1–3. Provides medical and scientific expertise to cross-functional teams and leads in protocol development and safety assessment.
Responsibilities
- Medical Monitoring: Contribute to and be a key member of Study Delivery Teams; lead medical data review and eligibility assessments; manage site interactions for medical questions and safety management guidelines; assess key safety-related serious adverse events with Worldwide Patient Safety; oversee safety narratives; provide medical oversight in protocol development and safety considerations; maintain GCP and training compliance.
- Clinical Development Expertise & Strategy: Design and develop clinical plans and protocols with strategic focus; provide medical accountability for a group of studies; lead benefit/risk analyses; partner with Clinical Scientists to support study execution (site activation, enrollment, and protocol adherence); identify and cultivate investigators and thought leaders; maintain strong medical reputation in the disease area and stay current with literature and regulatory developments; provide ongoing medical education to study teams.
- Health Authority Interactions & Publications: Serve as medical expert in Health Authority interactions and advisory boards; draft clinical content for CSRs, regulatory reports, briefing books, and submission documents in collaboration with CSs.
Qualifications
- Degree: MD required (or x-US equivalent).
- Experience: 5+ years of industry and/or clinical trials experience.
- Key Competencies: Clear communication and ability to lead scientific/clinical presentations; subspecialty training in applicable therapeutic area; strong scientific method knowledge (statistical design, analysis, interpretation); expertise in drug development; ability to execute robust clinical plans and protocols; strong leadership and teamwork.
Education
- MD required (or x-US equivalent).
Skills
- Medical data review and safety assessment
- Protocol development and input on inclusion/exclusion criteria
- Cross-functional collaboration and leadership
- Communication of complex scientific information
- Regulatory and health authority engagement