Clinical Research Coordinator

Role & responsibilities

A Clinical Research Coordinator (CRC) plays a crucial role in managing the day-to-day operations of clinical trials, ensuring they adhere to protocols, regulations, and ethical standards. Their primary responsibilities include recruiting participants, obtaining informed consent, collecting data, maintaining study documentation, and ensuring patient safety. CRCs work closely with Principal Investigators (PIs) and other research team members to ensure the smooth and successful completion of clinical trials.

• Developing and implementing study protocols.
• Ensuring adherence to Good Clinical Practice (GCP) and Institutional Review Board (IRB) regulations.
• Managing the overall workflow of the clinical trial, from planning to completion.
• Recruiting and screening potential participants.
• Obtaining informed consent from participants.
• Scheduling and coordinating study visits, procedures, and assessments.
• Monitoring participant safety and compliance with the study protocol.
• Reporting adverse events to the PI and sponsor.
• Collecting and managing study data accurately and thoroughly.
• Maintaining accurate and organized research documentation, including case report forms and informed consent documents.
• Entering data into electronic data capture systems (EDCs).

Preferred candidate profile

B. Pharm & M. Pharm candidates are preferred