Cancer Clinical Trials Coordinator | Data & Compliance

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

Job summary

UC Irvine's Chao Family Comprehensive Cancer Center is seeking an Assistant Clinical Research Coordinator to support Phase II–IV cancer trials. Under supervision, you will coordinate data, assist with recruitment and consent, and maintain trial records across protocols.

You will liaise with sponsors and regulatory bodies, ensure OnCore data integrity, and support reporting to NCI, IRB, and FDA while upholding GCP and institutional policies.

Qualifications

• Bachelor's degree required or equivalent experience.
• Experience coordinating clinical research with strong data skills.
• Familiarity with regulatory requirements (IRB, GCP).

Responsibilities

• Coordinate and manage data across multiple cancer protocols (Phase II-IV).
• Assist PI with recruitment, screening, consent, and questionnaires.
• Maintain trial documentation and regulatory records.
• Serve as liaison to sponsors and oversight bodies; communicate findings.
• Enter and verify data in OnCore; support reporting to NCI/IRB/FDA.

Skills

Interpersonal skills

Communication

Problem solving

Data management

Time management

Multi-tasking

Initiative

Team player

Attention to detail

Discretion/confidentiality

Record keeping

Critical thinking

Education

Bachelor's degree

Tools

OnCore

MS Office

Job description

UC Irvine's Chao Family Comprehensive Cancer Center is seeking an Assistant Clinical Research Coordinator to support Phase II–IV cancer trials. Under supervision, you will coordinate data, assist with recruitment and consent, and maintain trial records across protocols.

You will liaise with sponsors and regulatory bodies, ensure OnCore data integrity, and support reporting to NCI, IRB, and FDA while upholding GCP and institutional policies.