IQVIA UK’s RWE team is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across a diverse range of therapeutic areas. The CRA will cover sites across UK & Ireland, with 6-7 site visits per month.
Responsibilities include site monitoring visits, site training, and ensuring regulatory compliance. The role requires 1–2 years on-site monitoring experience, a degree in a scientific or health discipline, and strong knowledge of GCP/ICH guidelines.
CRA II: UK & Ireland Clinical Trials Monitor (Phase 3/4) in Reading employer: IQVIA, Inc.
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work with cutting-edge technology in the heart of the healthcare industry. Join us in a role that not only challenges you but also allows you to make a meaningful impact on global health outcomes.
