IQVIA's Medicines Evaluation Unit (MEU) in a hospital-based research facility is seeking an organised Clinical Trial Assistant. You will support CRAs and the RSU team by maintaining Trial Master File records, handling clinical documents, and coordinating trial supplies and data flow.
This office-based role offers exposure to multiple therapeutic areas and a collaborative team environment. Responsibilities include preparing and filing documentation, ensuring SOP compliance, and acting as a
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Clinical Trial Documentation & Compliance Assistant in Manchester employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
