Senior Clinical Research Coordinator — Trials & Compliance

UCI Health Regional Burn Center; Irvine (CA); On-site; USD 52,000 - 85,000; Full time

Job summary

UCI Center for Clinical Research seeks an experienced Clinical Research Coordinator to manage trials across multiple therapeutic areas. You will lead daily trial operations, ensure protocol adherence, and coordinate with investigators, sponsors and regulatory bodies.

You will handle data collection and documentation, maintain quality control, and support enrollment goals while ensuring patient safety and regulatory compliance in a busy research environment.

Qualifications

• Minimum 3 years of related work experience as a clinical research coordinator (CRC) or assistant CRC.
• Bachelor’s degree in related area or equivalent combination of education and/or experience.
• Experience coordinating Phase I–IV trials and regulatory submissions.

Responsibilities

• Lead day-to-day execution of assigned clinical trials across centers.
• Ensure accurate data collection, documentation, and compliance with GCP/ICH and FDA guidelines.
• Coordinate with sponsors, IRB, and study teams; manage study documentation and data in OnCore.

Skills

CRC coordination

IRB submissions

Data management

FDA regulations

Education

Bachelor’s degree in related area or equivalent

Tools

OnCore

EDC systems

Microsoft Office

Job description

UCI Center for Clinical Research seeks an experienced Clinical Research Coordinator to manage trials across multiple therapeutic areas. You will lead daily trial operations, ensure protocol adherence, and coordinate with investigators, sponsors and regulatory bodies.

You will handle data collection and documentation, maintain quality control, and support enrollment goals while ensuring patient safety and regulatory compliance in a busy research environment.