IQVIA in Reading, United Kingdom is seeking a Senior Clinical Research Associate (CRA) to lead on-site monitoring across PI sites within a cfSP framework. You will ensure patient safety, data integrity, and protocol adherence while building strong investigator relationships.
The role requires 4+ years of on-site monitoring in CRO/pharma settings, solid GCP/ICH knowledge, and the ability to travel up to 40–60% of the time.
Senior CRA, CFSP Specialist – Global Trials 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.
