Clinical Site Associate

Job description

Clinical Site Associate Germany ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. 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...