Danielle Littee, MPH, RAC, is currently a Principal Scientist at Merck, having previously served as a Senior Manager at Acceleron Pharma and Orchard Therapeutics. They led Emerging Markets Regulatory Affairs at Takeda Oncology from 2014 to 2018 and held various roles in regulatory affairs and analysis throughout their career. Danielle earned a Master of Public Health with a focus on Health Law, Bioethics, and Human Rights from Boston University and a Bachelor of Arts in Psychology from Stony Brook University.
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