IQVIA Biotech is seeking an on-site Clinical Research Monitor to join our team in the UK. You will perform site monitoring visits, manage recruitment plans, and ensure regulatory compliance across studies, particularly in Oncology.
Strong communication and organizational skills are essential. Responsibilities include training sites, tracking submissions and data queries, and maintaining trial documentation in line with GCP/ICH and local regulations.
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Oncology CRA II: Site Monitoring & Trial Execution 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.
