IQVIA Biotech is seeking an on-site Clinical Research Associate to monitor oncology studies across UK sites. You will coordinate visits, ensure GCP/ICH compliance, and support site recruitment and data management.
You will liaise with site staff, manage documentation, and contribute to trial success in a fast-paced environment. We require a Bachelor’s degree in a scientific field, 1 year of monitoring experience, strong English communication, and proficiency in Word, Excel and PowerPoint.
CRA II: Oncology Site Monitoring Specialist 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.
