Site Specialist I

Job description

Site Specialist I ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Site Specialist I to join our diverse and dynamic team. As a Site Specialist I at ICON, you will support investigator sites with key administrative and operational activities to help ensure clinical trials run smoothly, efficiently, and in compliance with applicable regulations. What You Will Be Doing: - Supporting the collection, review, and tracking of essential site documents in accordance with study requirements and SOPs. - Maintaining accurate site information and status updates in clinical trial management systems and trackers. - Assisting with site communications, meeting scheduling, and follow-up on outstanding actions. - Helping prepare materials for site visits, meetings, and audit or inspection activities. - Ensuring site-related documentation is filed correctly to support inspection readiness. - Collaborating with CRAs, Clinical Site Associates, and project teams to resol...