Erica Levine is a Project Manager in Memorial Sloan Kettering’s Office of Technology Development. She is a member of OTD’s Technology Management and Commercialization group.

Erica joined MSK in 2010, serving for seven years as an IND/IDE Project Manager in the Investigational Products Division / Core Facility. From 2008-2010, she was an Associate Director, Regulatory Affairs, at Asubio Pharmaceuticals, Inc., a subsidiary of Daiichi Sankyo. Previously, she served at Shire Human Genetic Therapies, Inc. (formerly Transkaryotic Therapies, Inc.) as a Regulatory Affairs Associate and Regulatory Project Manager. Earlier, she worked as a Project Manager at Pharmaceutical Information Associates, Ltd.

Erica received her Bachelor of Science degree in Health Studies from Boston University, Sargent College of Health and Rehabilitation Sciences in 1996.