IQVIA Biotech is seeking a qualified Clinical Research Associate to perform on-site monitoring visits and manage site performance on oncology studies. You will ensure protocol compliance, site training, and timely regulatory submissions while maintaining strong communication with sites and the study team.
The role requires a minimum of 1 year in on-site monitoring, familiarity with GCP/ICH guidelines, and solid English communication skills.
CRA II: Oncology Site Monitoring Specialist in Manchester 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.
