Assistant Regulatory Affairs Coordinator

🇺🇸 Orange, CA 🕑 Full-Time 💰 $30 - $49 per Hour 💻 Compliance 🗓️ June 27th, 2026

IRB Rive

Edtech.com's Summary

University of California, Irvine is hiring an Assistant Regulatory Affairs Coordinator to support regulatory aspects of clinical trials at the UCI Center for Clinical Research. The role involves managing multiple-phase research protocols, ensuring compliance with study protocols, maintaining documentation, and coordinating with regulatory bodies such as IRB and FDA.

Highlights

Manage regulatory components of clinical trials from initiation to completion.
Ensure compliance with Good Clinical Practice, SOPs, and university policies.
Maintain clinical trial documentation and investigator site files.
Report submissions and events to IRB, FDA, and sponsor monitors within required timeframes.
Work with clinical research teams and assist principal investigators on regulatory matters.
Use OnCore clinical trial management system and Microsoft Office suite including Outlook, Word, Excel, PowerPoint, Teams, and Zoom.
Require high organizational, communication, analytical, and problem-solving skills.
Minimum high school graduation with relevant experience; preferred research certifications (e.g. ACRP, SoCRA) and CITI training.
Salary range: $29.63 to $48.81 per hour.
May require occasional work outside normal hours and travel to off-site research locations.