IQVIA LLP is seeking an experienced Clinical Research Associate to perform on-site monitoring visits in the UK, ensure protocol adherence, and manage site communications. You will support recruitment planning, training, and documentation to maintain regulatory compliance and data integrity across interventional studies.
The role requires at least 2 years of on-site monitoring experience, a degree in a scientific discipline or health care, and full UK right to work, with visa sponsorship not
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Onsite Clinical Research Associate – Flexible Monitoring & Study Support 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.
