Clinical Project Manager- IVDC
About this role
About the Role Lead global study teams to ensure studies are designed, planned, conducted, monitored, and closed out within the planned timeline and budget, while ensuring sponsor responsibilities and regulatory compliance. Own the timeline and budget planning and execution, and provide oversight to outside support including CROs, consultants, and medical advisors. Foster cross-functional collaboration to drive successful study delivery. What You'll Do
- Leading the global study team with full accountability for study deliverables regarding quality, budget, and timelines.
- Developing key study documents (e.g., Design Validation Plan, protocol, study training materials, study forms and templates, study report).
- Overseeing planning and operational aspects of companion diagnostics studies sponsored by Pharma partners.
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