Clinical Research Coordinator: Lead Trials & Data

UC Irvine; Irvine (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

UC Irvine, through the UCI Center for Clinical Research, seeks a Clinical Research Coordinator to lead day-to-day trial execution, coordinate data management, and ensure regulatory compliance. You will interact with clinicians, sponsors, and IRB to maintain study integrity and patient safety.

The role requires coordinating multi-site trials, maintaining OnCore data, and preparing documentation for sponsors while adhering to FDA, GCP/ICH and internal SOPs.

Qualifications

• Bachelor’s degree or equivalent combination of education and experience.
• Minimum 3 years of related work experience as a clinical research coordinator.
• Experience with human subjects research and IRB submissions or approvals.
• Strong data management skills and attention to detail.
• Ability to read and understand clinical trial protocols and implement procedures.
• Familiarity with medical terminology and regulatory requirements (FDA, GCP/ICH).

Responsibilities

• Lead day-to-day execution of assigned clinical trials across multiple phases (I–IV).
• Coordinate data collection, transcription into CRFs and sponsor-specific EDC systems.
• Recruit patients, screen participants and monitor enrollment goals.
• Maintain compliance with GCP/ICH guidelines, SOPs and FDA regulations.
• Communicate with investigators, sponsors, IRB, and study monitors; prepare reports.

Skills

Clinical coordination

Data management

Communication (English)

Attention to detail

Education

Bachelor's degree

Tools

OnCore

Microsoft Office

Adobe Acrobat

Job description

UC Irvine, through the UCI Center for Clinical Research, seeks a Clinical Research Coordinator to lead day-to-day trial execution, coordinate data management, and ensure regulatory compliance. You will interact with clinicians, sponsors, and IRB to maintain study integrity and patient safety.

The role requires coordinating multi-site trials, maintaining OnCore data, and preparing documentation for sponsors while adhering to FDA, GCP/ICH and internal SOPs.