IQVIA is seeking an on-site Clinical Research Associate to support site monitoring across multiple sites in the United Kingdom. You will conduct monitoring visits, ensure GCP compliance, and manage essential trial documentation with the study team.
You will drive subject recruitment plans, train site staff, and maintain regular communication to manage expectations and issues. Strong English, organization, and time/financial management are essential.
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Senior Clinical Research Associate – On-Site Monitoring in Broughton 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.
