Erica Levine is a Senior 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, a subsidiary of Daiichi Sankyo. Previously, she served at Shire Human Genetic Therapies (formerly Transkaryotic Therapies) as a regulatory affairs associate and regulatory project manager. Earlier, she worked as a project manager at Pharmaceutical Information Associates.

Erica received her bachelor of science degree in health studies from Boston University, Sargent College of Health and Rehabilitation Sciences in 1996.