Oncology Clinical Trials Coordinator

University of North Carolina at Chapel Hill; Chapel Hill (NC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Professional training opportunities

Exclusive perks

Job summary

The University of North Carolina at Chapel Hill is seeking a Clinical Research Coordinator to advance cancer trials within the UNC / LCCC Clinical Trials Office. The role involves managing multiple oncology studies from activation to closure, under supervision, ensuring regulatory compliance and patient safety throughout the life cycle.

You will recruit and consent participants, coordinate visits across clinic settings, document procedures, and collaborate with research teams to maintain

Qualifications

• Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience.
• All degrees must be received from appropriately accredited institutions.
• Experience as a study coordinator or in oncology clinical trials is preferred.
• Familiar with Phase I-III clinical research; familiarity with investigation drugs and devices is a plus.
• SOCRA or ACRP certification is preferred.

Responsibilities

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

Skills

Clinical research experience

Study coordination

Regulatory knowledge

Data entry accuracy

Education

Bachelor’s degree in a related field

Job description

The University of North Carolina at Chapel Hill is seeking a Clinical Research Coordinator to advance cancer trials within the UNC / LCCC Clinical Trials Office. The role involves managing multiple oncology studies from activation to closure, under supervision, ensuring regulatory compliance and patient safety throughout the life cycle.

You will recruit and consent participants, coordinate visits across clinic settings, document procedures, and collaborate with research teams to maintain