Clinical Research Coordinator

The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical research studies under the supervision of a Principal Investigator (PI). This role ensures that studies are conducted according to the study protocol, regulatory requirements, and institutional policies while maintaining participant safety and data integrity.

Key Responsibilities

• Coordinate all aspects of assigned clinical trials, including participant recruitment, screening, enrollment, and follow-up.
• Obtain informed consent from study participants.
• Collect, record, and maintain accurate study data and documentation.
• Schedule and conduct study visits and procedures according to protocol.
• Communicate with sponsors, monitors, and regulatory bodies as needed.
• Prepare and submit regulatory documents, including IRB submissions and study updates.
• Maintain inventory of study supplies and manage investigational products (if applicable).
• Ensure compliance with Good Clinical Practice (GCP) and institutional standards.