IQVIA Biotech in the United Kingdom is seeking an experienced on-site Clinical Monitor to oversee oncology studies. You will conduct site visits, ensure protocol adherence, and maintain TMF/ISF documentation while coordinating with site staff and the study team.
The role requires 1 year of on-site monitoring experience, strong knowledge of GCP/ICH guidelines, and excellent English communication. A scientific or healthcare degree is preferred, with proficiency in MS Office and a willingness to
Oncology CRA II — Site Monitoring & Trial Oversight in Swillington 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.
