Overview Bristol Myers Squibb seeks an experienced Senior Clinical Trial Physician within Clinical Development. The role provides medical accountability and oversight for multiple clinical trials, with matrix management responsibilities across internal and external networks. It involves managing Phase 1–3 studies and offering medical and scientific expertise to cross-functional teams.
Responsibilities Medical Monitoring: contribute to and may be a member of a high-performing Study Delivery Team (SDT) or Clinical Development Team (CDT); lead medical data review of trial data, including eligibility; oversee site interactions for medical questions and education (safety management guidelines); assess safety-related serious adverse events in collaboration with Worldwide Patient Safety and oversee safety narratives; lead protocol development input with medical strategic oversight; fulfill GCP and compliance obligations for clinical conduct and maintain required training.
Clinical Development Expertise & Strategy: design and develop clinical plans and protocols with strategic focus based on asset/drug, disease area, and science; provide medical accountability for a group of studies; lead benefit/risk analyses in a matrix team with Clinical Scientists; partner with Clinical Scientists to support study execution (site activation, enrollment status, adjudication of deviations); identify investigators and thought leaders to gather input on emerging science; maintain a strong medical/scientific reputation in the disease area; monitor regulatory and competitive landscape; provide ongoing medical education with CS to support protocol-specific training for the study team and investigators.
Health Authority Interactions & Publications: act as medical point of expertise in Health Authority interactions and advisory board meetings; author or draft clinical content for CSRs, regulatory reports, briefing books, and submission documents in partnership with CSs.
Qualifications MD required (or x-US equivalent).
Experience 5 or more years of industry experience and/or clinical trials experience required.
Key Competencies Clear communication and ability to lead presentations in scientific and clinical settings.
Subspecialty training in applicable therapeutic area desired.
Expertise in scientific method, including statistical design, analysis, and interpretation; drug development process; ability to execute an effective clinical plan and protocols; strong leadership and teamwork capabilities.
Travel Domestic and international travel may be required.
Compensation & Benefits Compensation range varies by location; examples include Madison/Giralda, NJ and Princeton, NJ ranges of $275,630 – $333,998. Additional incentive cash and stock opportunities may be available. Benefits include medical, pharmacy, dental, vision, wellbeing programs, 401(k), disability and life insurance, paid holidays, vacation, volunteer days, parental and family support, tuition reimbursement, and recognition programs. Final compensation is based on experience and other factors.
Eligibility for specific benefits varies by job and location. For more on benefits, visit careers.bms.com/life-at-bms/.
On-site Protocol & Accessibility BMS has an occupancy model that defines where work occurs: site-essential (100% onsite), site-by-design (hybrid with at least 50% onsite), and field-based/remote-by-design (travel to visit customers, patients, or partners as needed). BMS provides accommodations for applicants with disabilities and directs inquiries to adastaffingsupport@bms.com. See careers.bms.com/eeo-accessibility for the Equal Employment Opportunity statement.
BMS recommends staying up to date with Covid-19 vaccines and boosters. Employment decisions consider applicants with arrest or conviction records as permitted by law. California residents: additional information is available at the California residents page.
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