Stephen Moore

Stephen started working as a medical writer in 2012, having completed a PhD in chemistry at the University of Southampton. His first medical writing role comprised a mixture of medical affairs and publications work within a medical communications agency based in Oxford. After a few years, he switched to regulatory writing within a large contract research organization. In his current role as a medical writing manager at Worldwide Clinical Trials, Stephen writes and reviews a broad range of regulatory documents, including informed consent materials, covering a variety of indications and trial phases.