IQVIA Biotech in the United Kingdom is seeking a Clinical Research Associate to perform on-site monitoring visits for oncology studies. You will ensure GCP/ICH compliance, manage site communications, and track recruitment and data quality to support trial progress.
Collaborating with study teams, you will prepare visit reports, resolve issues, and help maintain trial master file integrity. A background in life sciences, strong English communication, and solid organizational skills are essential;
Oncology Clinical Research Associate - Site Monitoring Pro in Pudsey 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.
