Kehinde Bakin, MS, PMP, is an accomplished regulatory affairs professional with extensive experience in submissions management and regulatory operations. Currently serving as Associate Director of Submissions Management at Novavax, part of Global Regulatory Operations since December 2021, Kehinde previously held the role of Senior Manager in the same area. Prior experience includes leading submission projects for Biogen and Bristol Myers Squibb at Parexel and serving as a Regulatory Submissions Project Manager at DXC Technology, where responsibilities included managing client projects and ensuring the quality of regulatory submissions. With a strong educational background including a Master's in Clinical Trial Sciences from Rutgers University, Kehinde has also contributed to regulatory processes at organizations such as Kinapse, Forest Laboratories, and Novartis.
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