IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor trials and ensure sites conduct studies according to the protocol and regulatory requirements. The role involves site visits, recruitment tracking, protocol training, TMF/ISF maintenance, data query resolution, and collaboration with the study team to ensure quality and timely delivery.
Applicants should have a Bachelor's degree in a scientific discipline or healthcare, at least 1 year of on-site monitoring
Clinical Research Associate II: Site Monitoring & Studies 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.
