IQVIA Biotech is seeking an on-site clinical monitor with oncology experience to join a dynamic team in the UK. You will conduct site visits, train sites on protocols, and ensure compliance with GCP/ICH guidelines while managing recruitment and study documentation end-to-end.
The role emphasizes strong communication, time and financial management, and collaboration with study teams. 3–4 years’ monitoring experience is expected, with a degree in science or healthcare.
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Senior CRA - Oncology Site Monitoring & Trials Impact 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.
