Senior CRA – Frontline Clinical Trial Monitoring in the UK

IQVIA LLC in the United Kingdom is seeking an experienced Clinical Research Associate to perform on-site monitoring visits, ensure GCP/ICH compliance, and support site start-up and ongoing study execution. You will collaborate with investigative sites, manage data and regulatory documentation, and help drive subject recruitment to meet project timelines.

The role requires 18 months of independent on-site monitoring, flexibility to travel, and a life science background.

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