Rebecca (Peggi) Drain

Rebecca (Peggi) Drain has worked in the pharmaceutical industry since 2007. Rebecca (Peggi) began their career at Bristol-Myers Squibb Co. as the Oncology Dossier Lead, providing global regulatory dossier guidance and designing tailored approaches for successful dossier strategies. Rebecca (Peggi) then progressed to the roles of Director Global Dossier Management and Associate Director. In 2019, they joined Intensity Therapeutics, Inc. as the Vice President of Regulatory Affairs and Quality Assurance, and was later promoted to Executive Director of Regulatory Affairs and Quality Assurance.

Rebecca (Peggi) Drain obtained a Bachelor of Science (BS) in Pathobiology from the University of Connecticut.