Cancer Trials Coordinator – Clinical Research

UC Irvine; California (MO); On-site; USD 60,000 - 90,000; Full time

Job summary

UC Irvine is seeking an Assistant Clinical Research Coordinator to support cancer-related trials across protocol phases II–IV. You will coordinate data collection, regulatory compliance, and patient recruitment under the Clinical Trials Unit.

The role requires collaboration with the PI, sponsors, and IRB/funding agencies, ensuring quality data and trial integrity. Ideal candidates have 1–3 years of CRC experience, strong communication, and the ability to multitask in a fast-paced,

Qualifications

• Bachelor's degree or equivalent experience in a related field.
• 1–3 years of clinical research coordination experience.
• Experience with cancer-related research preferred.

Responsibilities

• Coordinate phase II–IV cancer-related protocols per GCP, SOPs, and UC policies.
• Assist PI with recruitment, screening, consent, and scheduling.
• Maintain regulatory and data-management communications with sponsors and IRBs.

Skills

Communication

Data management

GCP

Regulatory knowledge

Teamwork

Multitasking

Clinical research coordination

Education

Bachelor's degree or equivalent experience

Tools

OnCore

Excel

PowerPoint

Microsoft Word

Job description

UC Irvine is seeking an Assistant Clinical Research Coordinator to support cancer-related trials across protocol phases II–IV. You will coordinate data collection, regulatory compliance, and patient recruitment under the Clinical Trials Unit.

The role requires collaboration with the PI, sponsors, and IRB/funding agencies, ensuring quality data and trial integrity. Ideal candidates have 1–3 years of CRC experience, strong communication, and the ability to multitask in a fast-paced,