Tim Dube is the Assistant Vice President for Regulatory Affairs for PCMA, joining with a deep history of experience in pharmaceutical and biotechnology policy issues. He represents PCMA before federal regulators in HHS and other Departments.

Prior to joining PCMA, Tim worked as a senior policy analyst within the US Department of Health and Human Services’ Office of the Assistant Secretary for Planning and Evaluation (ASPE). Previous to ASPE, Tim worked for 11 years with Genentech, in various roles spanning from drug development to commercialization to state and federal policy.

Tim graduated with a B.A. in Political Science from Boston College and an M.P.H. from Boston University.

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