Vice President, Global Program Lead - Hematology Late Development
$341,360–$413,648 year
On-site · Princeton, New Jersey, United States or Boudry, Neuchâtel, Switzerland
Job Summary
Vice President, Global Program Lead for Hematology Late Development accountable for two hematology assets, including a marketed asset for anemia and a CELMoD candidate for sickle cell disease. Leads the Global Program Teams and orchestrates the design and execution of a global integrated development plan from candidate nomination through drug development to launch and commercialization. Develops and inspires a high-performing matrix, maintains cross-functional stakeholder relationships, and inputs to upstream/downstream strategy as new data and competitive insights emerge. Responsibilities include defining the integrated development plan, participating in regulatory filings (NDA/BLA), leading program strategy and commercialization planning, building value propositions with market access considerations, supporting investor relations and public affairs, and integrating market inputs into the development plan to maximize asset value. Contributes to disease-area strategies (e.g., AML), engages with KOLs, and collaborates with Medical Affairs on KOL plans. Demonstrates leadership across global matrix functions, designs clinically differentiating trials, and translates clinical data into evidence for regulatory and commercial strategies. Requires broad understanding of domestic and international issues in the pharmaceutical industry, ability to influence across senior leaders, and track record of delivering large, complex drug development programs and trials.
Required Qualifications
- BS/BA required; advanced degree preferred (MD/PhD/MBA/PharmD, etc.)
- experience in the drug development process
- minimum of 10 years in the drug development and commercialization process with progression in relevant roles
- significant experience in related therapeutic area (hematology)
- experience in building development plans aligned with broader strategy
- ability to build and lead cross-functional stakeholder partnerships in a matrix organization
- knowledge of US and global pharmaceutical regulations
- ability to navigate complex healthcare environments
- prior submission experience highly preferred
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