RN Clinical Research Coordinator — RN role in Asheville, NC | Days, GCP/FDA-focused, ASAP start

Ref #: M-RN-296257

Join a collaborative clinical research team in Asheville, NC as a full-time Registered Nurse coordinating research studies. This day-shift position starts ASAP and involves managing study activity across the protocol lifecycle while ensuring participant safety and regulatory compliance.

Key responsibilities:

• Coordinate and oversee clinical research studies and protocols.
• Screen, enroll, and educate research participants; obtain informed consent.
• Collect, verify, and document clinical data and study results.
• Monitor patient safety, adverse events, and protocol adherence.
• Schedule and coordinate study visits, labs, and follow-up appointments.
• Maintain accurate study documentation and regulatory records.
• Collaborate with investigators, sponsors, research staff, and clinical care teams.
• Ensure compliance with Good Clinical Practice (GCP), FDA, and ethical standards.

Qualifications:

• Active RN license in good standing.
• Graduate of an accredited nursing program.
• BLS certification required.
• Previous clinical research experience and knowledge of GCP/FDA regulations preferred.
• Strong organizational, communication, and documentation skills.

Location: Asheville, NC
Employment type: Full-time
Shift: Days
Start date: ASAP