Senior Clinical Trials Coordinator

UC Irvine; California (MO); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Retirement plans

Employee discounts

Job summary

UC Irvine is seeking a Clinical Research Coordinator to oversee complex trials from initiation to completion. You will interview patients, screen participants, collect and coordinate data, and ensure strict adherence to GCP and SOPs while maintaining high-quality documentation.

Work closely with investigators and sponsors, manage data in sponsor CRFs and OnCore, and navigate regulatory processes and IRB submissions to support timely milestones.

Qualifications

• Bachelor’s degree in related area or equivalent combination of education and/or experience.
• Minimum 3 years of related work experience as a clinical research coordinator (CRC) or equivalent experience.
• Demonstrated track record of human subject's research coordination and IRB submissions.
• Experience working in a medical/clinical setting and familiarity with medical terminology.
• Excellent written and verbal communication skills in English.

Responsibilities

• Coordinate clinical trials from initiation through completion.
• Interview study patients, screen participants, and collect data per protocol.
• Maintain regulatory documentation and ensure GCP compliance and SOP adherence.
• Coordinate data submission to sponsors and ensure data quality for milestones.
• Maintain study information in the clinical trial management system (OnCore).
• Collaborate with Principal Investigators, coordinators, sponsors, and regulatory bodies.

Skills

Clinical research coordination

Data management

Communication skills

Microsoft Office

Team collaboration

Education

Bachelor’s degree in related area

Tools

OnCore

EDC systems

Job description

UC Irvine is seeking a Clinical Research Coordinator to oversee complex trials from initiation to completion. You will interview patients, screen participants, collect and coordinate data, and ensure strict adherence to GCP and SOPs while maintaining high-quality documentation.

Work closely with investigators and sponsors, manage data in sponsor CRFs and OnCore, and navigate regulatory processes and IRB submissions to support timely milestones.