IQVIA in Droylsden, UK is seeking experienced Clinical Research Associates to perform site monitoring visits and ensure compliance with regulatory requirements. The role involves evaluating study site practices and managing study progress while collaborating with project teams.
The ideal candidate will have at least 1 year of independent monitoring experience and a strong understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. This position is not eligible for UK visa sponsorship.
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