Responsibilities of a Clinical Research Coordinator

Clinical Research Coordinators (CRCs) have a variety of responsibilities related to the management of clinical trials. As key members of the clinical trial team, CRCs are responsible for the day-to-day management of the trial, ensuring the safety of participants, and collecting and managing data.

CRCs typically develop and manage study protocols, coordinate the activities of the research staff, and oversee the collection and reporting of data. They serve as primary contacts for research participants and must be knowledgeable of federal and local regulations governing clinical research.

The primary responsibilities of a Clinical Research Coordinator include:

• Developing and implementing study protocols • Coordinating the activities of research staff • Ensuring the safety of participants • Collecting and managing data • Monitoring the progress of the clinical trial • Ensuring compliance with federal and local regulations • Serving as the primary contact for research participants • Educating and providing support to research staff • Maintaining accurate records and documentation • Preparing reports and presentations related to the clinical trial • Collaborating with other members of the research team