Laura Hindle is an accomplished professional in regulatory affairs with a focus on oncology and virology, currently serving as Associate Director of Regulatory Affairs at Gilead Sciences since July 2016. With extensive experience in developing and executing regulatory strategies, Laura has successfully led initial EU Marketing Authorization Applications (MAAs) and provided cross-functional regulatory guidance, while managing a team. Prior to Gilead Sciences, Laura held roles at GSK, including Regulatory Project Manager, where the focus was on lifecycle management of anti-HIV products. Laura earned a Ph.D. in Molecular Biology, Immunology, and Cancer Research from the University of Birmingham, and a BSc Hons in Biochemistry from the University of Leeds.
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