IQVIA in Nottingham, UK is looking for experienced Clinical Research Associates to join their Site Management team. In this role, you will be responsible for performing site monitoring visits according to regulatory requirements, managing the progress of clinical trials, and ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Candidates should have experience in independent monitoring, knowledge of trial protocols, and a life sciences degree or equivalent experience. Note that this role is not eligible for UK visa sponsorship.
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