IQVIA Biotech in Colton, United Kingdom, is seeking an on-site Clinical Research Associate to monitor oncology studies in line with GCP/ICH guidelines. You will conduct site visits from initiation to close-out, ensure regulatory compliance, and maintain TMF/ISF documentation.
You’ll collaborate with study teams, track recruitment, manage data queries, and support start-up activities where needed. A bachelor’s in a scientific or healthCare field and at least one year of monitoring experience are
Oncology Clinical Research Associate — Site Monitoring Pro in Colton 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.
