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Director, Global Clinical Physician (Cardiovascular)

Bristol Myers Squibb
August 19, 2026
Full-time
Remote friendly (Cambridge, MA)
Worldwide
Clinical Research and Development
Role: Lead clinical/medical assessment and diligence for cardiovascular assets at Bristol Myers Squibb, supporting deal evaluation, portfolio strategy, and development planning. Responsibilities: serve as a scientific/clinical contact in due diligence, lead literature reviews, assess trial design and feasibility, develop clinical development plans, and provide medical input on safety and risk. Collaborate cross-functionally with Biostatistics, Regulatory, Medical Affairs, and Commercial teams; provide medical guidance to junior staff; escalate safety/risk issues impacting deal timelines. Requirements: MD with board certification or eligibility in cardiology or internal medicine; 6-8 years of clinical and/or industry experience with expertise in cardiovascular therapeutics, data interpretation, and clinical trial design. Key biopharma specifics: experience with early to late-phase cardiovascular development, safety risk assessment, portfolio valuation, and deal diligence. Advanced knowledge of GCP/ICH, clinical operations, and data review tools; proficiency in medical writing, strategic thinking, and cross-functional communication. Work setup: role may involve hybrid onsite work at Cambridge Crossing or NJ locations with flexible work arrangements.