Impactful Oncology Trials Coordinator

PeopleAdmin, Inc.; Chapel Hill (NC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits package

Paid leave

Professional training opportunities

Job summary

University of North Carolina is seeking a Research Coordinator to advance oncology clinical trials in compliance with federal regulations and institutional policies. You will independently manage multiple trials through activation, implementation, and closure under supervision.

Responsibilities include participant recruitment, coordinating visits, documentation, data entry, and ensuring patient safety through collaboration with research teams.

Qualifications

• Bachelor’s degree in a discipline related to the field and 1 year of related training or experience.
• Strong knowledge of ICH GCP and regulatory requirements.
• Experience coordinating oncology clinical trials and complex studies.
• Ability to manage data, documentation and regulatory submissions with accuracy.
• Excellent communication and teamwork for cross-functional collaboration.

Responsibilities

• Recruitment, consent, and enrollment of study participants.
• Coordinate study visits across clinic settings.
• Document procedures and visits, facilitate sample collection and data entry.
• Collaborate with research teams to ensure regulatory compliance and patient safety.

Skills

Clinical research coordination

Regulatory compliance

ICH GCP knowledge

Data management

Communication

Team collaboration

Education

Bachelor's degree in related field

Job description

University of North Carolina is seeking a Research Coordinator to advance oncology clinical trials in compliance with federal regulations and institutional policies. You will independently manage multiple trials through activation, implementation, and closure under supervision.

Responsibilities include participant recruitment, coordinating visits, documentation, data entry, and ensuring patient safety through collaboration with research teams.