Regional Clinical Study Manager
On-siteHome, Washington, United States
Job Summary
Lead regional clinical operations teams and external vendors to manage study delivery from feasibility through closeout within agreed timelines and budget. Plan and execute regional timelines, drive trial feasibility, and oversee site selection in collaboration with country heads and medical affairs. Ensure inspection readiness by monitoring protocol compliance, managing TMF quality, and preparing for regulatory audits. Collaborate with stakeholders to resolve escalated site issues, support Clinical Study Report planning, and manage regional budgets and vendor contracts. Provide performance feedback to team members and mentor junior staff while maintaining close alignment with global study goals.
Required Qualifications
- Bachelor's Degree in a scientific or healthcare discipline
- 4 or more years of progressive experience in clinical research within biotech, pharma or CRO industry
- Proven experience in clinical research including relevant experience as team lead in clinicial functions
Desired Qualifications
- Higher Degree
- Experience as CRA
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