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Program Manager
Job in
Princeton, Mercer County, New Jersey, 08543, USA
Listed on 2026-02-09
Listing for:
BCforward
Full Time
position Listed on 2026-02-09
Job specializations:
-
Management
Healthcare Management -
Healthcare
Healthcare Management, Healthcare Administration
Job Description & How to Apply Below
Job Title:
Program Manager – Drug Development (R&D)
Location: Princeton, NJ (Hybrid – 50% onsite at Princeton Pike)
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Duration: 13 months
Pay Rate: $115–$123.30/hr
Position SummaryWe are seeking an experienced Drug Development Program Manager to support global R&D drug development assets across the full lifecycle
. This is a true R&D Program Management role
, focused at the asset level
, partnering closely with Global Program Leads (GPLs) to drive strategy, planning, and execution from early development through regulatory submission.
This role is not an IT Project Manager, Clinical Trial Manager, or CMC Program Manager position.
Key Responsibilities- Partner closely with Global Program Leads to drive asset-level strategy, planning, and execution
- Own lifecycle management (LCM) planning for assigned drug development assets
- Drive multiple programs simultaneously, ensuring alignment on timelines, deliverables, and key decisions
- Lead cross-functional coordination and stakeholder alignment across R&D functions
- Support end-to-end registrational development
, from early development through submission (IND → NDA/BLA/MAA) - Develop and maintain integrated program plans, timelines, and risk mitigation strategies
- Communicate program status, risks, and opportunities to senior leadership and governance bodies
- Utilize program management tools including Planisware, MS Project, Tableau, and Microsoft Office
- B.S. degree in a scientific discipline (advanced degree preferred but not required)
- 8+ years of experience in R&D Drug Development Program Management
- Prior experience as a Drug Development Program Manager (or equivalent role)
- End-to-end drug development experience
, including full registrational exposure - Strong experience partnering with senior stakeholders and cross-functional teams
- Excellent communication, organization, and presentation skills
- Experience in immunology and/or cardiovascular therapeutic areas
- Experience working in large pharma, small biotech, or CRO environments
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