Clinical Site Associate ICON is a integral 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. Ensuring accurate filing and maintenance of essential documents to support inspection and audit readiness. Collaborating with internal stakeholders to support timely site

📌 Clinical Site Associate (Madrid)
🏢 Jobtome
📍 Madrid