IQVIA LLC in the United Kingdom is seeking an experienced Clinical Research Associate to perform on-site monitoring visits, ensure GCP/ICH compliance, and support site start-up and ongoing study execution. You will collaborate with investigative sites, manage data and regulatory documentation, and help drive subject recruitment to meet project timelines.
The role requires 18 months of independent on-site monitoring, flexibility to travel, and a life science background.
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Senior CRA - Frontline Clinical Trial Monitoring in the UK 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.
