Procom
Study Coordinator
Chapel Hill, North Carolina, United States · Onsite
POSTED
7/13/2026
Job Description
Study Coordinator:
On behalf of our Clinical Research client, Procom is searching for a Study Coordinator for a 6-month role. This position is an onsite position at our client’s Chapel Hill, NC office.
Study Coordinator - Job Description:
The Study Coordinator will manage multiple oncology clinical trials, ensuring they are conducted in compliance with Good Clinical Practice (GCP), federal regulations, and institutional policies. This role involves direct patient interaction and coordination of research activities across various locations within UNC Medical Center and the UNC-Chapel Hill campus.
Study Coordinator - Responsibilities:
• Independently manage multiple oncology clinical trials from startup through study closeout.
• Identify, screen, recruit, and enroll eligible research participants.
• Maintain accurate and complete source documentation.
• Coordinate collection, processing, storage, and shipment of research specimens.
• Ensure compliance with GCP, FDA regulations, IRB requirements, and UNC policies.
• Review billing calendars and submit participant reimbursement paperwork.
• Serve as a primary contact for assigned clinical trials and assist in training new staff members.
Study Coordinator - Mandatory Skills:
• Bachelor's degree in a related scientific, healthcare, or research discipline.
• Experience as a study coordinator or in oncology clinical trials.
• Knowledge of ICH GCP and federal regulations.
• Strong computer skills and ability to manage multiple projects.
• Effective verbal and written communication skills.
• Ability to work collaboratively in a team environment.
• Familiarity with medical terminology and data abstraction.
Study Coordinator – Nice-to-Have Skills:
• SOCRA or ACRP certification.
• Experience with Phase I-III clinical research.
• Prior involvement in coordinating complex studies independently.
• High attention to detail in data gathering and documentation.
• Experience in process improvement and quality initiatives.
Study Coordinator – Assignment Length:
This is a 6-month assignment.
Study Coordinator - Start Date:
ASAP.
Study Coordinator - Assignment Location:
Chapel Hill, NC, fully onsite.
Ready to apply?
You'll complete the application through our portal.
Role summary
Study Coordinator
Chapel Hill, North Carolina · Onsite
TYPE
Contract · 6 Months
STARTS
7/27/2026
POSTED
2 days ago
ATS ID
328183
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