Clinical Research Data Coordinator — Oncology Trials

UCI; California (MO); On-site; USD 65,000 - 90,000; Full time

Job summary

University of California, Irvine (UCI) seeks an Assistant Research Data Coordinator to support data management for cancer trials at the Chao Family Comprehensive Cancer Center. Under supervision, you will collect and coordinate data across Phase I–IV protocols, ensuring accuracy, regulatory compliance, and timely sponsor submissions.

You will collaborate with clinicians and study staff, maintain trial data in OnCore, and assist with regulatory reporting while upholding strict confidentiality and

Qualifications

• Bachelor’s degree required; 1-3 years of clinical research coordination preferred.
• Experience with cancer-related research is a plus.
• Ability to read medical terminology and patient charts accurately.

Responsibilities

• Support data management for Phase I–IV cancer trials in CFCCC.
• Coordinate data submission to study sponsors and ensure quality control.
• Transcribe data into case report forms and sponsor ED C systems.
• Communicate with sponsors, regulatory bodies, and national groups as needed.
• Maintain trial information in OnCore and adhere to policies and guidelines.

Skills

Communication

Multitasking

Data management

Team collaboration

Attention to detail

Problem solving

Independent initiative

Education

Bachelor’s degree (BA/BS)

Tools

OnCore

Microsoft Office

Job description

University of California, Irvine (UCI) seeks an Assistant Research Data Coordinator to support data management for cancer trials at the Chao Family Comprehensive Cancer Center. Under supervision, you will collect and coordinate data across Phase I–IV protocols, ensuring accuracy, regulatory compliance, and timely sponsor submissions.

You will collaborate with clinicians and study staff, maintain trial data in OnCore, and assist with regulatory reporting while upholding strict confidentiality and