IQVIA in Maidenhead, UK, seeks a Senior Clinical Research Associate to conduct on-site monitoring across studies in the UK. You will support site initiation, conduct ongoing monitoring visits and ensure quality and compliance with GCP/ICH guidelines.
The role requires 18 months of independent monitoring experience, strong knowledge of GCP/ICH, and willingness to travel to diverse investigative sites. Visa sponsorship is not available for this position.
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Senior CRA: Lead Site Monitoring & Trial Delivery in Maidenhead 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.
