Assistant Clinical Data Coordinator, Cancer Trials

UC Irvine

California (MO)

On-site

USD 65,000 - 85,000

Full time

3 days ago
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Benefits offered by this job

Medical insurance
Retirement savings plans
Employee discounts and perks

Job summary

UC Irvine's Chao Family Comprehensive Cancer Center seeks an Assistant Research Data Coordinator to support data management for cancer protocols (Phase I–IV). The role entails accurate data collection, CRF transcription into sponsor EDCS, and timely submissions to sponsors.

You will work with the clinical research team, PIs, and sponsors, ensuring regulatory adherence and data quality, with OnCore as the trial management system and NCI reporting compliance.

Qualifications

  • Working knowledge of medical terminology and ability to read progress notes in patient charts.
  • Experience coordinating clinical data collection and data entry.
  • Familiarity with GCP, SOPs, and regulatory requirements.

Responsibilities

  • Provide comprehensive data management for cancer-related protocols across Phases I–IV.
  • Ensure timely, accurate data submission to study sponsors and maintain CRF data in sponsor EDCS.
  • Liaise with sponsors, governing agencies, and multicenter networks; support study teams and PIs.
  • Maintain trial information in the trial management system (OnCore) and comply with NCI reporting requirements.

Skills

Medical terminology
Data management
Communication skills
Time management
Teamwork
Attention to detail
Microsoft Office
Clinical data collection

Education

Bachelor of Arts/Bachelor of Science

Tools

OnCore

Job description

UC Irvine's Chao Family Comprehensive Cancer Center seeks an Assistant Research Data Coordinator to support data management for cancer protocols (Phase I–IV). The role entails accurate data collection, CRF transcription into sponsor EDCS, and timely submissions to sponsors.

You will work with the clinical research team, PIs, and sponsors, ensuring regulatory adherence and data quality, with OnCore as the trial management system and NCI reporting compliance.

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