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Stuart Grant, PhD, serves as the Senior Vice President of Regulatory Affairs at NuCana plc since December 2015, where responsibilities include regulatory leadership for clinical development activities and medical writing for various regulatory submissions. Previously, Stuart held roles at inVentiv Health Clinical as Director of Study Start-Up, managing global oversight of Phase II-III trial performance, and at ClinTec International as Director of Regulatory & Technical Services, overseeing regulatory affairs and medical writing. Additional experience includes regulatory consultancy at Kendle International and medical writing at Complete Medical Communications. Stuart's academic background includes a PhD in Physiology & Pharmacology and a BSc (Hons) in Immunology & Pharmacology, both from the University of Strathclyde.