IQVIA in the United Kingdom seeks a Senior Clinical Research Associate to conduct site qualification, initiation, monitoring and close-out visits in line with protocol, GCP and ICH guidelines. You will ensure patient safety, data integrity, and protocol compliance across sites.
Responsibilities include maintaining site relationships, monitoring regulatory documentation, recruitment activity, and data queries, with travel up to 40-60%.
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Senior Clinical Research Associate – Global Trials in Preston 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.
