IQVIA is seeking a Senior Clinical Research Associate to conduct site qualification, initiation, monitoring and close-out visits in line with GCP and ICH guidelines across the UK & Ireland. You will ensure patient safety, data integrity, protocol compliance, and build strong investigator relationships while supporting recruitment and site performance.
Travel up to 40–60% is required. You will maintain inspection-ready documentation and collaborate with cross-functional teams to achieve study
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Senior CRA: Strategic Clinical Trial Monitoring in Langley 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.
