IQVIA, Medicines Evaluation Unit (MEU) Ltd, is seeking an administrative professional to support Clinical Research Associates and Regulatory and Start-Up teams. The role focuses on updating and maintaining Trial Master Files and related documents, with responsibilities spanning document handling and archiving, as well as coordination of trial supplies and data flow.
The ideal candidate has 2-3 years of relevant experience, solid English communication, and a commercial mindset.
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Clinical Trial Admin & Documentation Specialist 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.
