Phase II-IV Cancer Trials Coordinator

University of California, Irvine; Orange (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

The University of California, Irvine's Chao Family Comprehensive Cancer Center is seeking an Assistant Clinical Research Coordinator to support Phase II–IV cancer trials through data management, participant coordination, and regulatory compliance.

Under supervision, you will recruit, screen, consent, collect data, and liaise with sponsors, IRB, and FDA, while maintaining OnCore records and ensuring Good Clinical Practices.

Qualifications

• Bachelor's degree or equivalent; 1–3 years clinical research coordination experience preferred.
• Ability to coordinate multiple cancer-related protocols and maintain documentation.
• Strong communication, organization, and data management skills.
• Familiarity with GCP, SOPs, and regulatory compliance.

Responsibilities

• Coordinate all aspects of Phase II–IV cancer trials per GCP and SOPs; data collection and record keeping.
• Attend clinic with PI to assist recruitment, screening, and administering questionnaires.
• Serve as liaison to sponsors, agencies, and research networks; communicate with IRB, FDA, and monitors.
• Maintain trial information in OnCore and ensure reporting aligns with NCI guidelines.

Skills

Multitasking under deadlines

Excellent communication

Data management

Team collaboration

Education

Bachelor's degree or equivalent (1-3 years experience)

Tools

OnCore

Microsoft Office

Job description

The University of California, Irvine's Chao Family Comprehensive Cancer Center is seeking an Assistant Clinical Research Coordinator to support Phase II–IV cancer trials through data management, participant coordination, and regulatory compliance.

Under supervision, you will recruit, screen, consent, collect data, and liaise with sponsors, IRB, and FDA, while maintaining OnCore records and ensuring Good Clinical Practices.