Clinical Site Associate

Job description

CSA role, office based hybrid, Poland 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 As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards. What You Will Do: You will contribute to scientific operations activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: - Supporting site activation activities, including the collection, review, and tracking of essential documents and approvals. - Maintaining up-to-date site information and status in clinical trial management systems and trackers. - Assisting CRAs and project teams with site communications, follow-up, and resolution of site-level queries. - Coordinating logistics for site visits and meetings, including scheduling, documentation preparation, and follow-up actions. - Ensuring accurate filing and maintenance of essential documents...