IQVIA Biotech in Livingston, United Kingdom, is seeking a Clinical Monitor to support on-site visits, ensure adherence to GCP/ICH guidelines, and manage site communications across oncology studies. You will conduct site monitoring visits, support recruitment plans, and help establish strong relationships with study sites to drive trial progress.
The role requires at least 1 year of on-site monitoring experience, a biomedical or health-care degree, and solid knowledge of regulatory requirements.
CRA 2: Oncology Site Monitoring Expert in Livingston 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.
