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IRB Program Manager
Job Summary
A company is looking for an IRB Program Manager to supervise clinical research trials and ensure compliance with IRB policies and regulations.
Key Responsibilities
- Coordinate review and approvals of research proposals to ensure compliance with IRB requirements
- Interact with governmental agencies regarding research regulations and participate in audits as necessary
- Oversee day-to-day IRB functions, including document pre-review and distribution of meeting materials
Required Qualifications
- Experience in clinical research and IRB processes
- Knowledge of federal, state, and institutional regulations regarding human subjects research
- Ability to provide regulatory and methodological guidance to research investigators
- Experience in developing and implementing training programs related to regulatory guidelines
- Supervisory experience, including oversight and mentorship of staff
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COMPLETE JOB DESCRIPTION
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