VP, Global Program Lead - Cell Therapy
Bristol Myers Squibb
June 25, 2026
Remote friendly (Princeton, NJ)
United States
Clinical Research and Development
Position Summary:
- Lead two novel multiple myeloma cell therapy programs as Global Program Lead (GPL), accountable from candidate nomination through drug development, launch, and commercialization.
- Orchestrate global integrated program strategy; lead cross-functional global program teams and a high-performing matrix; manage upstream/downstream alignment and business implications; advance BMS multiple myeloma disease area strategy.
Responsibilities:
- Define and execute strategic integrated development plans; manage regulatory filings (NDA/BLA) and engagement with Health Authorities/Advisory Committees.
- Develop program and clinical strategy, commercialization strategy, and business cases; ensure access, pricing, and reimbursement needs inform trial design.
- Integrate commercialization inputs (market/labeling, forecasts, risk, valuations) to enable approval of differentiated assets and maximize asset value.
- Design, execute, and interpret competitively differentiating clinical trials; set endpoints with Health Authorities; translate data into scientific/publication and commercial strategies.
- Lead commercialization/CMCs needs (e.g., trade packaging); support KOL plans and Medical Affairs engagement.
- Inclusive cross-matrix leadership, enterprise mindset problem-solving, accountability, and values-driven leadership.
Qualifications:
- BS/BA required; advanced degree preferred (MD/PhD/MBA/PharmD).
- Drug development process experience; ≥10 years across drug development & commercialization with progression.
- Demonstrated leadership (build/lead high-performing team) and significant therapeutic area experience.
- Preferred/Additional: end-to-end development expertise; matrix stakeholder partnership; influence senior leaders; US/global regulatory knowledge; cross-geography collaboration; complex project execution; prior submission and prior cell therapy experience.
Benefits (as stated):
- Health coverage (medical/pharmacy/dental/vision); wellbeing programs; 401(k) and insurance/disability.
- Paid time off (flexible time off/annual vacation varies by location/role).
Application:
- If the role doesn’t perfectly match your resume, BMS encourages you to apply anyway.
- Lead two novel multiple myeloma cell therapy programs as Global Program Lead (GPL), accountable from candidate nomination through drug development, launch, and commercialization.
- Orchestrate global integrated program strategy; lead cross-functional global program teams and a high-performing matrix; manage upstream/downstream alignment and business implications; advance BMS multiple myeloma disease area strategy.
Responsibilities:
- Define and execute strategic integrated development plans; manage regulatory filings (NDA/BLA) and engagement with Health Authorities/Advisory Committees.
- Develop program and clinical strategy, commercialization strategy, and business cases; ensure access, pricing, and reimbursement needs inform trial design.
- Integrate commercialization inputs (market/labeling, forecasts, risk, valuations) to enable approval of differentiated assets and maximize asset value.
- Design, execute, and interpret competitively differentiating clinical trials; set endpoints with Health Authorities; translate data into scientific/publication and commercial strategies.
- Lead commercialization/CMCs needs (e.g., trade packaging); support KOL plans and Medical Affairs engagement.
- Inclusive cross-matrix leadership, enterprise mindset problem-solving, accountability, and values-driven leadership.
Qualifications:
- BS/BA required; advanced degree preferred (MD/PhD/MBA/PharmD).
- Drug development process experience; ≥10 years across drug development & commercialization with progression.
- Demonstrated leadership (build/lead high-performing team) and significant therapeutic area experience.
- Preferred/Additional: end-to-end development expertise; matrix stakeholder partnership; influence senior leaders; US/global regulatory knowledge; cross-geography collaboration; complex project execution; prior submission and prior cell therapy experience.
Benefits (as stated):
- Health coverage (medical/pharmacy/dental/vision); wellbeing programs; 401(k) and insurance/disability.
- Paid time off (flexible time off/annual vacation varies by location/role).
Application:
- If the role doesn’t perfectly match your resume, BMS encourages you to apply anyway.