Oncology Clinical Research 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 in Chapel Hill, NC seeks a Study Coordinator to support oncology clinical trials under the UNC Lineberger Comprehensive Cancer Center. This on-site role involves coordinating visits, enrolling participants, collecting samples, and maintaining regulatory compliance in collaboration with the research team.

Required is a Bachelor's degree with at least a year of related experience; Oncology trial exposure is preferred.

Qualifications

• Bachelor’s degree in a related field and at least one year of related experience or equivalent training.
• Experience in oncology clinical trials and study coordination preferred.
• Knowledge of ICH GCP and federal regulations; familiarity with medical records and terminology.

Responsibilities

• Recruitment, consent, and enrollment of study participants
• Coordination of study visits across clinic settings
• Documentation of procedures and visits, sample collection, and data entry
• Collaboration with research teams to ensure regulatory compliance and patient safety

Skills

Clinical Research

Regulatory Knowledge

Communication

Education

Bachelor's degree

Tools

ICH GCP

SOCRA/ACRP certification

Job description

The University of North Carolina at Chapel Hill in Chapel Hill, NC seeks a Study Coordinator to support oncology clinical trials under the UNC Lineberger Comprehensive Cancer Center. This on-site role involves coordinating visits, enrolling participants, collecting samples, and maintaining regulatory compliance in collaboration with the research team.

Required is a Bachelor's degree with at least a year of related experience; Oncology trial exposure is preferred.