Study Coordinator — Oncology Clinical Trials

Job overview

The Study Coordinator — Oncology Clinical Trials role is onsite in Chapel Hill, NC, with compensation not specified. The position coordinates research activities across the client’s medical center, campus locations, and affiliated clinics. The client is a public research university. The coordinator manages oncology trials through activation, enrollment, conduct, monitoring, and closure, helping ensure protocol compliance and participant safety. The role connects investigators, sponsors, research staff, and clinical teams while maintaining study data and regulatory documentation.

What you'll do

• Manage multiple oncology trials from startup through closeout
• coordinate activation, monitoring, and study visits
• recruit, screen, enroll, and educate participants
• conduct informed consent discussions
• maintain source records and enter data
• resolve data queries
• coordinate specimen collection, processing, storage, and shipment
• maintain regulatory compliance
• report serious adverse events
• support audits, billing documentation, and team training.

What we're looking for

Skills & competencies

study coordinator

oncology clinical trials

chapel hill nc

clinical research

participant recruitment

informed consent

gcp

irb

biospecimens

eclaro

Work arrangement

• Weekend coverage required

Benefits & perks

• 401(k) retirement savings plan
• pretax commuter benefits
• eligibility to purchase medical, dental, and vision insurance through ECLARO.

Why this role

The posting prefers experience as a study coordinator or in oncology clinical trials, including Phase I–III research. The role may involve exposure to bloodborne pathogens, biohazardous specimens, and other healthcare materials.

About the employer

ECLARO is hiring for this role. Industry: Colleges, Universities, and Professional Schools. Sector: 61.