Clinical Research Coordinator

GNP Research

Cooper City, FLFull-time

Behavioral Health Market Context

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Job Description

t, 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

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

Benefits

    Responsibilities

    • The ideal candidate is detail-oriented, proactive, and committed to ensuring protocol compliance and participant safety
    • 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


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