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Brendan Watson, MS, currently serves as a Senior Associate in Regulatory Affairs at BeiGene, having joined the company in August 2021. Previously, Brendan held positions at Progenity, Inc. as a Regulatory Affairs Specialist and Clinical Trials Associate, where responsibilities included developing study tracking systems and coordinating clinical trial documentation and site qualifications. Brendan's experience also includes a tenure as a Clinical Research Coordinator at GenomeDx Biosciences Inc., overseeing study master files and sample workflows, as well as a role at Thermo Fisher Scientific focused on manufacturing under strict compliance guidelines. Brendan holds a Master of Science in Biotechnology Regulatory Affairs from the University of Maryland Global Campus and a Bachelor of Science in Engineering from Arizona State University.