Cancer Trials Coordinator — OnCore Data & IRB Liaison

UCI; California, Northern (MO, KY); Hybrid; USD 52,000 - 75,000; Full time

Benefits offered by this job

Medical insurance

Retirement savings plans

Paid time off

Job summary

UC Irvine is seeking an Assistant Clinical Research Coordinator to support cancer trials in the CFCCC. You will assist the PI with patient recruitment, screening, and data collection, ensuring adherence to GCP, SOPs, and institutional policies. This role involves multi-site coordination and regulatory liaison.

The position requires collaboration with the Clinical Trials Unit, sponsors, and IRB, FDA, and other bodies. Strong organizational and communication skills are essential.

Qualifications

• BA/BS or equivalent experience required.
• Experience in clinical research coordination helpful.
• Experience with cancer-related research preferred.

Responsibilities

• Coordinate Phase II–IV cancer trials per GCP and SOPs.
• Maintain data in the clinical trial management system (OnCore).
• Support recruitment, screening, and patient questions in clinics.
• Serve as liaison to sponsors, regulators, and monitoring entities.
• Prepare reports and maintain compliant trial documentation.

Skills

Interpersonal communication

Organizational skills

multitasking

Data management

Microsoft Office

Attention to detail

Problem solving

Education

Bachelor of Arts/Bachelor of Science

Tools

OnCore

Excel

Word

Job description

UC Irvine is seeking an Assistant Clinical Research Coordinator to support cancer trials in the CFCCC. You will assist the PI with patient recruitment, screening, and data collection, ensuring adherence to GCP, SOPs, and institutional policies. This role involves multi-site coordination and regulatory liaison.

The position requires collaboration with the Clinical Trials Unit, sponsors, and IRB, FDA, and other bodies. Strong organizational and communication skills are essential.