Clinical Research Data Coordinator — Cancer Trials

UC Irvine; Orange (CA); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Retirement savings plans

Job summary

UC Irvine is seeking an Assistant Research Data Coordinator to support CFCCC’s cancer trials. You will manage data collection, ensure quality control, and prepare CRFs for sponsor submissions using sponsor-specific EDC systems.

You will collaborate with Principal Investigators and study coordinators, maintain trial information in OnCore, and ensure compliance with GCP, NCI, and FDA guidelines while protecting patient confidentiality.

Qualifications

• Bachelor's degree with 1–3 years clinical research coordination experience.
• Experience with cancer-related research.
• Strong communication and organizational skills.
• Knowledge of regulatory guidelines (IRB, FDA, NCI).

Responsibilities

• Manage data collection and quality control for cancer trials.
• Compile and transcribe data into case report forms (CRFs) for sponsor EDCS.
• Maintain accurate trial information in the OnCore system.
• Serve as liaison to sponsors, regulatory bodies and study teams.
• Ensure compliance with GCP and institutional policies.

Skills

Medical terminology

High-level communication

Data management

CRF preparation

Team collaboration

Microsoft Office

Education

Bachelor's degree (BA/BS) in related field

Tools

OnCore

EDC systems

Job description

UC Irvine is seeking an Assistant Research Data Coordinator to support CFCCC’s cancer trials. You will manage data collection, ensure quality control, and prepare CRFs for sponsor submissions using sponsor-specific EDC systems.

You will collaborate with Principal Investigators and study coordinators, maintain trial information in OnCore, and ensure compliance with GCP, NCI, and FDA guidelines while protecting patient confidentiality.