California Licensed Clinical Research Associate

Job Summary

A company is looking for an In-house Clinical Research Associate.

Key Responsibilities:

• Support clinical operations across multiple studies while ensuring subject safety and data integrity
• Review and maintain the electronic Trial Master File (eTMF) in compliance with SOPs, GCP, and ICH guidelines
• Serve as a liaison between internal teams, CROs, vendors, and investigator sites

Required Qualifications:

• Bachelor's degree preferred
• 3 years of experience in clinical research
• Experience as an unblinded CRA required
• Minimum 2 years of experience with site management and CRO/vendor oversight
• Prior biotech or pharmaceutical industry experience required