IQVIA Laboratories is looking for an experienced Clinical Research Associate to join their Site Management team in Stafford, UK. In this pivotal role, you will perform site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines while managing the overall progress of assigned studies.
The ideal candidate will have at least 1 year of independent on-site monitoring experience of interventional studies in the UK and strong communication skills to work effectively with sites and study team members.
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