California Licensed Clinical Research Associate
Job Summary
Managing multiple research protocols, the full-time California Licensed Clinical Research Associate I will ensure regulatory compliance and efficient protocol documentation while attending clinics as needed and receiving mentorship from experienced staff.
Key responsibilities
- Manage multiple research protocols to support efficiency and regulatory compliance
- Notify investigators of protocol changes and maintain current protocol materials
- Compile and submit regulatory documents for IRB, DSMB, and PRMC/CPRMC review
Required qualifications
- Associate's Degree
- One year of experience working in a healthcare setting, preferably in research
- Experience may substitute for minimum education requirements
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