Description
The Study Coordinator will plan and monitor the execution of assigned Phase I–IV clinical research protocols, including patient eligibility, study procedures, data collection and entry, adverse-event tracking, protocol deviations, source-documentation review, monitor visits, sponsor and FDA audit preparation, and reporting. The role requires knowledge of clinical trial data, FDA guidelines, and GCP, along with at least one year of experience in healthcare, research, or a related science field and at least one year of experience planning and managing clinical trial processes.
