Remote Oncology Clinical Trials Data Coordinator

The Rector & Visitors of the University of Virginia; Charlottesville (VA); Remote; USD 49,000 - 54,000; Full time

Job summary

The Rector & Visitors of the University of Virginia’s Comprehensive Cancer Center, Office of Clinical Research, seeks a Research Data Coordinator to support data entry, documentation, and records management for oncology clinical trials. This administrative role focuses on entering, organizing, and maintaining study data, not statistical analysis.

The position collaborates with disease teams, research coordinators, and principal investigators to maintain accurate study data and respond to data

Qualifications

• Bachelor's degree required; relevant experience may be considered in lieu of a degree.
• One to two years of relevant experience.
• Licensure not required.

Responsibilities

• Enter clinical research data from paper case report forms into appropriate databases.
• Learn and use multiple electronic databases according to study requirements.
• Address data queries from study management with coordinators or investigators.
• Extract required clinical information from medical charts and EMRs.
• Upload imaging data to study portals.
• Use DocuSign to obtain signatures on source documents.
• Organize and file research documents in study binders.
• Prepare routine cover letters and sponsor documentation.
• Maintain clinical trial data documentation to support daily operations.
• Provide administrative planning for clinical research data activities.
• Perform other duties as assigned.

Education

Bachelor's degree

Job description

The Rector & Visitors of the University of Virginia’s Comprehensive Cancer Center, Office of Clinical Research, seeks a Research Data Coordinator to support data entry, documentation, and records management for oncology clinical trials. This administrative role focuses on entering, organizing, and maintaining study data, not statistical analysis.

The position collaborates with disease teams, research coordinators, and principal investigators to maintain accurate study data and respond to data