California Licensed Clinical Research Associate

Job Summary

Supporting ongoing clinical trials, the in-house Sr Clinical Research Associate will ensure subject safety and data integrity while managing clinical operations in a hybrid role based in San Diego, California.

Key responsibilities:

• Support clinical operations across multiple studies, ensuring compliance with SOPs, GCP, and ICH guidelines
• Review and maintain the electronic Trial Master File (eTMF) and assist with regulatory documentation and site readiness
• Serve as a liaison between internal teams, CROs, vendors, and investigator sites, tracking enrollment and treatment status

Required qualifications:

• Bachelor's degree preferred
• 3 years of CRA experience with site management and CRO/vendor oversight
• Proficiency with Microsoft Office and Veeva eTMF required
• Experience in Phase I-III clinical trials
• Familiarity with Smartsheet and SharePoint is a plus