This full-time Clinical Research Coordinator role supports Phase I through IV trials within CenExel's specialized research centers, focusing on areas such as psychiatry, dermatology, and neurology. The position involves coordinating patient involvement from study initiation to completion, organizing research data, and ensuring strict adherence to ICH and GCP regulations. Key duties include observing subjects, performing safety assessments like vital signs and blood draws, reporting adverse events, and assisting with protocol development and staff training. The role offers a collaborative work environment that emphasizes teamwork, positive leadership, and work-life balance, with opportunities for professional growth in a respected facility. The position is based on-site in an office setting with a standard Monday through Friday schedule, though occasional overnight travel for training may be required.