IQVIA UK's cFSP team is growing and seeks an experienced Clinical Research Associate to perform on-site monitoring visits (selection, initiation, monitoring and close-out) in interventional studies in line with GCP and ICH guidelines, within the contracted scope of work.
You will collaborate with site staff and the study team to drive subject recruitment plans, administer protocol training, manage regulatory submissions and data queries, maintain TMF/ISF files, and produce visit reports and
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