Senior Director, Global Clinical Physician - Oncology

Bristol Myers SquibbCambridge Crossingonsite$351k–$425kView the original posting at Bristol Myers Squibb ↗

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Position Summary The Senior Director, Global Clinical Physician is the primary source of medical accountability and oversight for one or more Oncology clinical trials within the Drug Development organization. The incumbent will be accountable, alongside the Clinical Development Program Lead, for the development of differentiated and strategic clinical development plans from phase I expansion through to registrational execution. They will be foundational in working with teams in Research, Early and Late Development, providing insights into biology, translational elements, as well as overall benefit risk assessments. This role includes support of cross-portfolio activities in line with Clinical Excellence, including Protocol Review Committee, support of Business Development activities and Quality and compliance leadership. The Senior Director, Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. The Senior Director, Global Clinical Physician will report directly to the Clinical Development Program Lead or Head of Clinical Development. Key Responsibilities • Serves as a primary source of medical accountability and oversight for multiple clinical trials or a single trial with significant complexity within [TA] Clinical Development group • Supervises the development, monitoring, analysis, and interpretation of clinical trials and will supervise and have accountability for the clinical components of regulatory filings. • Will contribute to overall Therapeutic Area disease strategy while ensuring an overall portfolio view • Provides strategic insights into clinical development plans • Provides medical and scientific expertise to cross-functional BMS colleagues • Matrix management responsibilities across the internal and external network • Manages Phase 1 to Phase 3 clinical studies, with demonstrated decision-making capabilities • The role will be foundational in working with teams in Research, Early and Late Development teams to support gated investment decisions and transitions, providing insights into biology, translational elements as well as overall benefit risk assessments Clinical Development Expertise & Strategy: • A Senior Director, Global Clinical Physician is a tenured drug developer who can independently design and construct clinical development plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets. • Done in conjunction with Clinical Development Program Lead or as a delegate when CDPL is not assigned • Extensive experience in Research and Development (late and/or early development) and across various Phases of study design • Respected for Disease Expertise (internal to BMS and within the medical community) • Disease Lead- able to serve as internal consultant for respective disease(s) based on scientific knowledge and therapeutic expertise • Provides oversight and medical accountability for a group of high-priority studies • Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Global Clinical Scientists (CS) • Partners with CS to support executional delivery of studies • Existing stro

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