IQVIA in Manchester is seeking a qualified candidate for a site monitoring role focusing on independent on-site monitoring of clinical trials. The ideal candidate will have experience managing clinical trial protocols, in-depth knowledge of GCP and ICH guidelines, and a relevant life sciences degree. Responsibilities include conducting site visits, managing ongoing project communications, and ensuring adherence to regulatory practices. Flexibility to travel is essential. Note: this role is not eligible for UK visa sponsorship.
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