About this role
Temporary Clinical Research Coordinator (CRC) at University of California, Irvine. Location: Irvine or Orange or Orange County. Role: coordinating trials, screening participants, managing data Requirements: 2+ years CRC experience, knowledge of clinical research processes and GCP, strong data management and documentation skills, ability to follow complex protocols, effective communication, and English proficiency. Category: Research and Development (R&D) Seniority: Entry Level Tools: Electronic Data Capture (EDC) Commitment: Full Time, Temporary Workplace: Onsite Languages: English