Senior Data Coordinator, Oncology Trials

The University of North Carolina at Chapel Hill; Chapel Hill (NC); On-site; USD 56,000 - 65,000; Full time

Job summary

The University of North Carolina at Chapel Hill seeks a Data Coordinator to support oncology trials by accurately collecting and abstracting clinical data in compliance with GCP and regulatory requirements. This role oversees data activities across multiple studies under supervision.

Responsibilities include data entry, reconciliation, and ensuring audit readiness, with collaboration across study teams and regulatory staff.

Qualifications

• Bachelor’s degree or equivalent combination of training and experience.
• Experience in clinical data abstraction and data entry preferred.
• Knowledge of ICH GCP and federal regulations preferred.

Responsibilities

• Abstraction of clinical information from medical records and source documents to meet protocol specific requirements
• Collection and entry of study required data, ensuring completeness, accuracy, and timely submission
• Ongoing data reconciliation and query resolution to ensure data integrity
• Collaboration with study teams, regulatory staff, and clinical coordinators to support protocol compliance and patient safety
• Compilation and maintenance of research patient records, ensuring adherence to documentation standards, data reporting timelines, and audit-readiness
• This position is essential to the mission of the UNC / LCCC Clinical Trials Office, upholding research quality, supporting regulatory compliance, and safeguarding institutional integrity while contributing to discoveries that shape the future of cancer care.

Skills

Data abstraction

Clinical data collection

Data entry

Regulatory compliance

Team collaboration

Attention to detail

Education

Bachelor’s degree or equivalent

Job description

The University of North Carolina at Chapel Hill seeks a Data Coordinator to support oncology trials by accurately collecting and abstracting clinical data in compliance with GCP and regulatory requirements. This role oversees data activities across multiple studies under supervision.

Responsibilities include data entry, reconciliation, and ensuring audit readiness, with collaboration across study teams and regulatory staff.