Oncology Clinical Trials Coordinator

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

Benefits offered by this job

Medical insurance

Paid time off

Retirement plans

Employee discounts

Job summary

University of California, Irvine is seeking a Clinical Research Coordinator to support Phase I–IV cancer protocols. Under supervision, you will coordinate study activities, data collection, and regulatory compliance.

Responsibilities include assisting the PI with recruitment, consents, and questionnaires, maintaining trial documents, and interfacing with sponsors, IRB, FDA, and OnCore. Strong communication, organizational skills, and the ability to work in a dynamic, deadline-driven environment

Qualifications

• Bachelor's degree or higher with 3–5 years of related coordination experience.
• Experience coordinating cancer trials (Phase I–IV).
• Strong communication and organizational abilities.
• Proficiency with data management and regulatory compliance (IRB, FDA, sponsor communications).
• Experience with clinical trial management systems, preferably OnCore.

Responsibilities

• Coordinate all aspects of Phase I–IV cancer trials and ensure GCP compliance.
• Assist PI with recruitment, consent, questionnaires, and scheduling.
• Manage data collection, trial documentation, and record keeping.
• Communicate with sponsors and regulatory bodies and coordinate multi-site networks.
• Maintain OnCore entries and ensure reporting to NCI.

Skills

Interpersonal skills

Record keeping

Multitasking

Attention to detail

Communication skills

Critical thinking

Time management

Education

Bachelor degree

Tools

OnCore

Microsoft Office

Job description

University of California, Irvine is seeking a Clinical Research Coordinator to support Phase I–IV cancer protocols. Under supervision, you will coordinate study activities, data collection, and regulatory compliance.

Responsibilities include assisting the PI with recruitment, consents, and questionnaires, maintaining trial documents, and interfacing with sponsors, IRB, FDA, and OnCore. Strong communication, organizational skills, and the ability to work in a dynamic, deadline-driven environment