A leading clinical research organization in Royal Tunbridge Wells is looking for a Site Monitor to perform site visits, ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, and manage monitoring documentation. The ideal candidate will have at least one year of experience in independent on-site monitoring in the UK. Strong communication skills and an understanding of clinical research regulations are essential. Note: This role is not eligible for UK visa sponsorship.
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