Job Description

We are seeking a Clinical Research Coordinator (CRC) to assist with the day-to-day operations of clinical trials. The CRC will work closely with investigators, sponsors, and study participants to ensure that trials are conducted according to regulatory requirements and study protocols.

Key Responsibilities:

• Coordinate and manage clinical trial activities from start-up to close-out
• Recruit, screen, and consent study participants
• Schedule study visits and collect data during each visit
• Maintain accurate and complete study documentation
• Ensure compliance with study protocols, IRB guidelines, and GCP
• Handle investigational product (IP) per protocol (if applicable)
• Communicate with sponsors, CROs, and regulatory bodies as needed
• Support data entry and query resolution

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