IQVIA Biotech in the United Kingdom seeks an experienced on-site Clinical Research Associate to perform site monitoring visits, drive subject recruitment plans, and ensure GCP/ICH compliance. You will administer protocol training, establish regular communication with sites, and manage data queries and documentation.
The role requires at least one year of on-site monitoring, with oncology study experience preferred.
Oncology Clinical Research Monitor (On-site) in Scarcroft employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
