Data Coordinator

UNC-Chapel Hill•Chapel Hill, NC

About The Position

This position supports cancer research and improved patient outcomes by accurately collecting and abstracting clinical data for oncology trials in compliance with federal regulations, Good Clinical Practice, and institutional policies. Under the direction of a Clinical Operations Manager, the Data Coordinator independently oversees data-related activities for multiple complex studies throughout their life cycle, including activation, implementation, monitoring, and closure. The role supports the UNC / LCCC Clinical Trials Office by upholding research quality, supporting regulatory compliance, safeguarding institutional integrity, and contributing to discoveries in cancer care.

Responsibilities

  • Abstract clinical information from medical records and source documents to meet protocol-specific requirements.
  • Collect and enter study-required data, ensuring completeness, accuracy, and timely submission.
  • Conduct ongoing data reconciliation and resolve queries to ensure data integrity.
  • Collaborate with study teams, regulatory staff, and clinical coordinators to support protocol compliance and patient safety.
  • Compile and maintain research patient records in accordance with documentation standards, data reporting timelines, and audit-readiness requirements.
  • Oversee data-related activities for multiple complex studies through activation, implementation, monitoring, and closure.
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