Tavis B. is an experienced regulatory professional currently serving as Associate Director of Regulatory Operations at Rocket Pharmaceuticals, with a proven track record in regulatory affairs spanning over a decade. Prior roles include Associate Director of Publishing Operations at bluebird bio and Associate Director of Global Regulatory Affairs at LEO Pharma, where Tavis developed extensive expertise in submission requirements across the US, EU, and ROW markets. Tavis has a history of managing cross-functional teams, overseeing compliant global submissions, and leading publishing activities while maintaining strong technical interactions with health authorities. Educational qualifications include an ongoing Master of Science in Biopharmaceutical Regulatory Affairs from Northeastern University and a Bachelor of Arts in English Language and Literature from Elizabethtown College.
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