JOB SUMMARY

The Clinical Research Coordinator (CRC) is responsible for supporting the planning, coordination, and execution of clinical trials and research studies, ensuring compliance with regulatory requirements, Good Clinical Practice (GCP), and company standards.
This position requires prior experience in clinical research and strong working knowledge of regulatory compliance, study protocols, and participant coordination.
The candidate will participate in all research study related activities and quality assurance of data for assigned research projects.
The CRC works closely with the Principal Investigator and cross-functional teams to ensure high-quality, compliant research conduct.

• Coordinate study start-up activities, including IRB submissions and regulatory document preparation
• Enter and manage data in EDC systems, resolve queries, and maintain audit-ready documentation
• Track and report adverse events, deviations, and compliance issues
• Liaise with sponsors, CROs, and institutional departments to support study operations
• Maintain subject logs, regulatory binders, and study-related documentation
• Prepare for and participate in monitoring visits and audits
• Coordinate with internal teams and external vendors/CROs to ensure timelines and quality objectives are met
• Maintains inventory of study supplies and equipment
• Coordinates reimbursement for study subjects
• Screen, recruit, and consent participants in accordance with protocol and GCP
• Conduct study visits and collect source documentation including medical histories, vital signs, and assessments
• Other job functions as assigned
  Requirements: