GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and committed to ensuring protocol compliance and participant safety.
Key Responsibilities:
Oversee all aspects of clinical trials from start-up to close-out
Coordinate patient visits, informed consent, and data collection
Ensure regulatory compliance and accurate documentation
Liaise with sponsors, CROs, and internal teams
Qualifications:
2+ years of experience as a CRC in a clinical research setting
Strong understanding of GCP, FDA regulations, and IRB processes
Excellent organizational and communication skills
