Clinical Trial Coordinator

Job Summary

We are looking for a detail-oriented Clinical Trial Coordinator to support the planning, coordination, and execution of clinical trials in compliance with study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements.

Key Responsibilities

• Coordinate daily clinical trial activities and maintain study documentation.
• Assist Principal Investigators and clinical research teams with trial-related activities.
• Maintain Investigator Site Files (ISF) and essential clinical trial documents.
• Coordinate patient recruitment, screening, scheduling, and follow-up visits.
• Ensure informed consent forms and study records are properly maintained.
• Assist with data entry, query resolution, and clinical trial documentation.
• Coordinate with investigators, sponsors, Clinical Research Associates (CRAs), and site staff.
• Track study timelines, patient visits, and protocol compliance.
• Support adverse event documentation and reporting as per study requirements.
• Ensure confidentiality of patient information and compliance with GCP.