Role Overview
The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, managing Phase 1 to Phase 3 studies with demonstrated decision making capabilities. The role has matrix management responsibilities across the internal and external network and provides medical and scientific expertise to cross‑functional BMS colleagues.
Responsibilities
* Medical Monitoring
o Team Leadership & Collaboration – 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, including inclusion/exclusion criteria and safety considerations.
o Medical Monitoring & Safety – Lead medical and eligibility data reviews, assess safety‑related serious adverse events in partnership with Worldwide Patient Safety, and oversee site interactions and safety narratives.
o GCP & Compliance – Uphold all GCP obligations for clinical conduct, safety management guidelines, and maintain up‑to‑date required training.
* Clinical Development Expertise & Strategy
o Clinical Strategy & Protocol Design – Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols, focusing on drug/asset knowledge, disease area science, and regulatory targets.
o Medical Oversight & Accountability – Provide medical accountability across a group of studies, leading benefit/risk analyses within a matrix team environment alongside Clinical Scientists.
o Study Execution & Delivery – Partner with Clinical Scientists to support all aspects of study delivery, including site activation, enrollment, and adjudication of protocol violations and deviations.
o Stakeholder Engagement & Thought Leadership – Build and maintain relationships with principal investigators and key opinion leaders to inform emerging science, biomarker research, and clinical program design.
o Scientific Expertise & Education – Maintain deep, up‑to‑date knowledge of the disease area through conference attendance and literature review, staying informed on the competitive landscape and providing ongoing protocol‑specific medical education to study teams and investigators.
* Health Authority Interactions & Publications
o Health Authority & Advisory Engagement – Serve as the medical point of expertise in key Health Authority interactions and advisory board meetings.
o Regulatory Writing & Submissions – Author and draft clinical content for CSRs, regulatory reports, briefing books, and submission documents, including clinical narratives, in partnership with Clinical Scientists.
Qualifications and Experience
* MD required (or equivalent).
* Five or more years of industry experience and/or clinical trials experience.
* Ability to communicate information clearly and lead presentations in scientific and clinical settings.
* Subspecialty training in an applicable therapeutic area desired.
* Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation.
* Expertise in the drug development process and in executing an effective clinical plan and protocols.
* Strong leadership skills with proven ability to lead and work effectively in a team environment.
* Domestic and international travel may be required.
EEO and Employment Rights Statement
Bristol Myers Squibb is Disability Confident, a recognized employer. Qualified applicants with arrest and conviction records will be considered for employment pursuant to applicable laws. We will never request payments, financial information, or social security numbers during our application or recruitment process. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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