Clinical Research Coordinator 251215

A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring study protocols are followed, patient safety is maintained, and data is accurately collected. They act as the primary liaison between participants, researchers, and sponsors, handling study visits, regulatory documentation, and participant recruitment.

Key Responsibilities:

• Participant Management: Recruit, screen, and enroll patients, obtain informed consent, and schedule study visits.
• Data Collection & Entry: Accurately document study data in electronic case report forms (eCRFs) and maintain source documents.
• Protocol Adherence: Ensure all study procedures follow Good Clinical Practice (GCP) guidelines and study protocols.
• Safety Reporting: Identify and report adverse events (AEs) and serious adverse events (SAEs) promptly.
• Regulatory Documentation: Prepare and submit regulatory documents to IRBs and sponsors