IQVIA Biotech in the United Kingdom seeks a site monitor with 1–2 years of on-site monitoring experience, especially in oncology trials. You will ensure quality, compliance with GCP/ICH, and effective collaboration with clinical sites.
Your role includes coordinating site training, tracking recruitment, and maintaining TMF/ISF documentation, with potential involvement in start-up and contract-based financial tasks. English proficiency is essential.
CRA II: Oncology Trials Monitoring & Site Oversight 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.
