Sr. Clinical Research Associate

Job description

Sr. Clinical Research Associate 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 Sr. CRA at ICON, you will oversee and manage clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards. What You Will Do: Your focus will be on coordinating clinical trial monitoring delivery, resolving issues, and developing team capability. Key responsibilities include: Leading site management activities, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and regulatory guidelines. Serving as the primary point of contact for clinical sites, addressing site queries, and resolving issues to maintain site engagement and performance. Ensuring the integrity of clinical data by conducting thorough source data verification, reviewing site records, and monitoring for protocol devia...