Clinical Research Coordinator

Job Description

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