
This Clinical Research Associate role at ICON plc supports the Utah-based team in managing investigational sites across the southeast region. The position involves serving as the primary liaison between sites and sponsors, conducting various site visits including initiation and monitoring, and ensuring strict compliance with ICH-GCP regulations. Key responsibilities include maintaining accurate documentation in clinical systems, monitoring patient safety data, resolving data queries, and overseeing drug accountability. The role appeals to professionals seeking a career in a world-leading healthcare intelligence organization that fosters an inclusive culture, rewards high performance, and offers comprehensive benefits focused on well-being and work-life balance. Candidates must be willing to travel up to 50% for on-site monitoring visits.






















