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VP, Global Program Lead – Cell Therapy
Job in
Fall River, Bristol County, Massachusetts, 02720, USA
Listed on 2026-07-14
Listing for:
Jobtailor
Full Time
position Listed on 2026-07-14
Job specializations:
-
Healthcare
Healthcare Management
Job Description & How to Apply Below
- The Global Program Lead (GPL) will serve as the “point of accountability” for two novel cell therapies in multiple myeloma.
- These programs include ongoing pivotal studies with potential to redefine the treatment paradigm.
- The GPL role is accountable for leading the Global Program Teams and orchestrating the design and execution of a global integrated program strategy from candidate nomination through drug development to successful launch and commercialization.
- The GPL develops, leads, and inspires a high performing matrix.
- They are responsible for cross-functional stakeholder relationships and input to ensure end to end understanding of upstream and downstream alignment and business implications for the strategy, and its evolution as emerging data and competitive insights unfold.
- Integrates market inputs into the integrated development plan, including clinical plans and labeling strategy; appreciates translation of clinical data into claims and considerations for label development.
- BS/BA required, and an advanced degree preferred (MD, PhD, MBA, PharmD, etc.)
- Must have experience in the drug development process.
- Proven demonstrated leadership capability; previous experience in building and leading a high performing team.
- A minimum of 10 years in the drug development & commercialization process with proven progression in relevant roles.
- Significant experience in related therapeutic area.
- Extensive working knowledge in the end-to-end drug development process, along with expertise in one or more of the relevant areas.
- Prior experience in building a development plan that was aligned with a broader strategy (TA/Franchise) and endorsed by governance.
- Experience in building trusting cross-functional stakeholder partnerships in a matrix organization.
- Demonstrated ability to constructively influence peers and senior leaders across the enterprise.
- Working knowledge of regulations in the pharmaceutical industry (US and Global preferred).
- Demonstrated ability to effectively collaborate across geographic and functional boundaries (e.g. early development, R&D, disease strategy teams, marketing, access, etc.) and building strong external relationships.
- Ability to navigate through a complex and dynamic healthcare environment.
- Track record of successfully executing on large, complex projects, with a preference for successful drug trial oversight and execution.
- Abreast of scientific issues as they impact business development and strategic planning.
- Success in situations requiring rigorous, analytical problem solving and the ability to determine scientific opportunity and commercial targets.
- Broad understanding of domestic and international issues relative to the pharmaceutical industry.
- Proven agility in prioritizing and navigating competing demands.
- Prior submission experience is preferred.
- Prior cell therapy experience is preferred.
- BS/BA
- MD
- PhD
- MBA
- PharmD
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