Role OverviewThe Clinical Program Manager (CPM) is a key member of Clinical Operations and will closely partner with the Senior Director of Clinical Program Management. The CPM will provide regional and vendor oversight across a global Phase 3 program, helping drive consistent study execution, operational quality, and inspection readiness across regions, CROs, vendors, and study sites.
What You Will Do
Provide Clinical Operations oversight across assigned regions, CROs, and vendors within a large, global Phase 3 program, ensuring consistent execution against study plans, timelines, quality expectations, and regulatory requirements.
Why It Might Be a Fit
The ideal candidate will have at least 8+ years of relevant clinical research experience and a BS, BA, BN in a relevant scientific discipline or an RN (2 or 3 year certificate).
Requirements
- At least 8+ years of relevant clinical research experience
- BS, BA, BN in a relevant scientific discipline or RN (2 or 3 year certificate)
- MASH (formerly NASH), MASLD, and/or metabolic disease experience preferred
- Demonstrated experience with regional study oversight, CRO/vendor management, and operational performance
- Experience supporting clinical trial inspection and audit readiness, including identification and remediation of operational or documentation gaps
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