Clinical Research Coordinator
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
• 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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