Clinical Research Coordinator

Joint and Muscle Medical Care•Charlotte, NC

38d•$20 - $25•Onsite

About The Position

We are seeking an Experienced Clinical Research Coordinator to support the conduct of clinical trials across multiple therapeutic areas. The ideal candidate is detail‑oriented, proactive, and comfortable managing study visits independently while maintaining exceptional participant care and regulatory compliance.

Requirements

Associate’s degree in a health‑related field or nursing certificate/degree (LPN, RN, BSN with clinical experience)
Minimum 1+ year of experience as a Clinical Research Coordinator
Proficiency with EDC systems (Rave, Inform) and Microsoft Office
Ability to perform vitals, ECGs, phlebotomy, and sample processing
Strong understanding of GCP, ICH, FDA regulations, and IRB processes
Excellent communication, organization, and time‑management skills

Nice To Haves

Experience in oncology, immunology, cardiology, or CNS
Familiarity with PK/PD sampling or complex visit schedules
Experience with eReg systems (Veeva)
Bilingual skills

Responsibilities

Manage day‑to‑day study operations, ensuring strict adherence to protocol, GCP, and site SOPs.
Recruit, screen, consent, and schedule participants; conduct study visits and assessments.
Lead the consent process with clarity, accuracy, and ethical compliance.
Maintain complete, audit‑ready source documents and reconcile with EDC entries.
Enter high‑quality data, resolve queries promptly, and meet sponsor deadlines.
Assist with IRB submissions, essential documents, delegation logs, and training records.
Process, label, centrifuge, freeze, and ship biological samples per protocol.
Document and report AEs/SAEs; collaborate with investigators on assessments.
Prepare for monitoring visits, respond to findings, and maintain professional communication.
Track inventory, maintain equipment logs, and ensure visit readiness.