IQVIA is seeking experienced Clinical Research Associates to join our Site Management team in the UK. The role involves performing site monitoring visits, ensuring regulatory compliance and data integrity, and coordinating with investigative sites to support study timelines.
You will administer protocol training, track submissions and recruitment, and maintain essential TMF/ISF records while collaborating with the study team to manage expectations and issues.
Clinical Research Associate II: Flexible Work & Growth in Manchester 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.
