Oncology Clinical Trials Study Coordinator

The University of North Carolina at Chapel Hill; Chapel Hill (NC); On-site; USD 64,000 - 75,000; Full time

Job summary

The University of North Carolina at Chapel Hill is seeking a Study Coordinator to facilitate oncology clinical trials, manage data, and ensure compliance with Good Clinical Practice and institutional policies. The role supports the UNC/LCCC Protocol Office and requires patient safety focus and meticulous record-keeping.

Primary duties include coordinating subject visits, data management, and regulatory documentation.

Qualifications

• Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience.
• All degrees must be received from appropriately accredited institutions.
• SOCRA / ACRP Certification is desirable for role and advancement.

Responsibilities

• Facilitate conduct of oncology clinical trials in accordance with regulations and policies.
• Assist with subject recruitment, screening, enrollment and follow-up visits.
• Navigate medical records and perform data extraction to ensure accurate research data.

Skills

Therapeutic clinical research

Phase I–III clinical research

Data extraction

Study coordinator experience

Oncology clinical trials

Education

Bachelor’s degree in related field

SOCRA/ACRP Certification

Job description

The University of North Carolina at Chapel Hill is seeking a Study Coordinator to facilitate oncology clinical trials, manage data, and ensure compliance with Good Clinical Practice and institutional policies. The role supports the UNC/LCCC Protocol Office and requires patient safety focus and meticulous record-keeping.

Primary duties include coordinating subject visits, data management, and regulatory documentation.