Kimmi

​A Study Coordinator manages the day-to-day operations of clinical research studies, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. They coordinate participant visits, obtain informed consent, collect and document study data, and manage study supplies and investigational products. Study Coordinators also assist with participant recruitment and screening, support timely enrollment, and serve as a key liaison between investigators, sponsors, and CROs. Through careful oversight and strong communication, they help ensure participant safety, data integrity, and the overall success of clinical research studies.