California Licensed Clinical Research Analyst
Job Summary
To support the Human Research Protection Program, the full-time California Licensed Clinical Research Analyst will analyze and review regulatory submissions, provide support to the Institutional Review Board (IRB), and serve as a liaison between researchers and the IRB in a remote capacity.
Key responsibilities
- Analyze and review full-board and expedited regulatory submissions related to human subjects research
- Provide support to IRB members and ensure compliance with regulatory and institutional requirements
- Serve as a resource for researchers conducting studies within the health system
Required qualifications
- 4 years of experience in a health-related field or research, or an equivalent combination of education and experience
- 3 years of experience with IRB, regulatory, or research processes
Complete Job Description
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