Pharmaceutical Project Manager
Core
Primary customer-facing leader managing end-to-end CDMO client projects across the full product lifecycle from pre-clinical development through Phases I–IV and lifecycle management.
Role type
Senior IC pharmaceutical project manager (CDMO)
Builds
Clinical drug development projects for pharma, biopharma, and consumer health companies
Domain
Pharmaceutical manufacturing / CDMO / cGMP
Required skills
Project management in cGMP environment, Client relationship management, Cross-functional execution, Risk and escalation management, Phase gate review and approval coordination, Regulatory compliance knowledge
Preferred skills
PMP certification, Experience in FDA-regulated CDMO company, Scientific background (Chemistry, Biology, Pharmacy, Engineering)
Technologies
Microsoft Project, Outlook, Excel, Word, PowerPoint, WorkFront
Responsibilities
Serve as single point of contact for assigned CDMO clients, Manage client relationships including hosting site visits and governance meetings, Monitor and manage customer satisfaction, Ensure timely follow-up on decisions, risks, and deliverables, Escalate critical path issues impacting schedule, cost, quality, or compliance, Coordinate phase gate review and approval prior to clinical manufacturing
Seniority
Senior, hands-on IC