About the role
The Clinical Research Coordinator (CRC) is responsible for coordinating and managing the day-to-day operations of clinical trials, ensuring compliance with protocols and regulations. This role involves patient recruitment, data collection and management, regulatory documentation, and communication with investigators, sponsors, and other study personnel. The CRC plays a crucial role in the successful execution of clinical research studies, contributing to the advancement of scientific knowledge and patient care. This position may involve assisting with study start-up activities, monitoring patient adherence to study protocols, managing investigational product, and preparing study reports. Strong organizational skills, attention to detail, and knowledge of Good Clinical Practice (GCP) guidelines are essential for this role.