California Licensed Clinical Research Associate

Job Summary

To support clinical trials in Alameda, CA, the part-time Clinical Research Associate will conduct Phase I-IV studies, write study protocols, and monitor site adherence while managing CRF processing and data cleanup.

Key responsibilities

• Conduct Phase I-IV studies in compliance with Federal Regulations and ICH guidelines
• Write study protocols and ensure timely patient enrollment while monitoring site adherence
• Assist senior staff with study planning, designing CRFs, and managing CROs

Required qualifications

• Bachelor's Degree with 3+ years of experience at the CRA or CRC level
• Experience with site monitoring on the sponsor side
• Experience with medical device or in-vitro device studies