Cancer Trials Coordinator — Clinical Research Lead

UCI Health Regional Burn Center; Irvine (CA); On-site; USD 52,000 - 85,000; Full time

Job summary

UC Irvine's Comprehensive Cancer Center (CFCCC) is seeking a Clinical Research Coordinator to support cancer trials across Phase I–IV, ensuring compliance with GCP and SOPs. You will coordinate patient screening, recruitment, consent, data collection, and chart preparation in OnCore.

The role requires strong organizational skills, ability to work with multidisciplinary teams, and attention to regulatory guidance from IRB, FDA, and sponsors. Onsite in Irvine, CA with potential travel.

Qualifications

• Bachelor's degree or higher or equivalent experience.
• 3–5 years of related work coordination experience.
• Experience with cancer trials and OnCore is preferred.
• Strong communication and data management skills.

Responsibilities

• Coordinate Phase I–IV cancer protocols across sites.
• Assist PI with recruitment, screening, consent, and questionnaires.
• Prepare and maintain source documents and case report forms.
• Ensure regulatory compliance with IRB, FDA, and sponsor requirements.

Skills

Interpersonal skills

Communication

Data management

Multitasking

Team coordination

Problem solving

Attention to detail

Education

Bachelor's degree or equivalent experience

Tools

OnCore

Microsoft Office

Job description

UC Irvine's Comprehensive Cancer Center (CFCCC) is seeking a Clinical Research Coordinator to support cancer trials across Phase I–IV, ensuring compliance with GCP and SOPs. You will coordinate patient screening, recruitment, consent, data collection, and chart preparation in OnCore.

The role requires strong organizational skills, ability to work with multidisciplinary teams, and attention to regulatory guidance from IRB, FDA, and sponsors. Onsite in Irvine, CA with potential travel.