Research Data Coordinator

4 weeks ago

Orange, California, United States University Of California Irvine Full time
About the Role

The University of California, Irvine is seeking a highly skilled Research Data Coordinator to join our team. As a key member of our clinical research team, you will play a critical role in supporting the clinical research efforts of the Chao Family Comprehensive Cancer Center.

Key Responsibilities
  • Provide comprehensive data management for a research portfolio of Phase I-IV cancer-related protocols according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures.
  • Collect and coordinate data submission to study sponsors, ensuring quality control and timely milestone payments.
  • Compile and transcribe research patient data and study-related information into case report forms (CRFs) into sponsor-specific electronic data capture systems (EDC).
  • Work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of cancer-related trials.
  • Maintain communication with all elements of a multi-level research network, interacting with sponsoring agencies, including the National Cancer Institute, and compliance and regulatory groups, such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors.
Requirements
  • 1-3 years of related clinical research coordination work experience with a Bachelor of Arts/Bachelor of Science, or equivalent experience.
  • Demonstrated experience in maintaining flexibility and adaptability while implementing institutional change.
  • Ability to work independently, take initiative, and follow through on assignments.
  • Strong attention to detail and ability to multitask and meet deadlines.
  • Working knowledge of computer software, including Microsoft Office (Outlook, Word, Excel, and PowerPoint).
  • Ability to think critically, compile data from various sources, analyze data, and prepare reports.
Preferred Qualifications
  • Experience with clinical trial management systems, preferably OnCore.
  • Experience with cancer-related research.
  • Knowledge of various types of human subject clinical trials, including National Group, industrial, and Investigator-authored trials.
What We Offer

The University of California, Irvine offers a competitive salary range of $24.95-$31.37 per hour, as well as a comprehensive benefits package, including medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks.

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