Emily was raised in Sussex County, NJ and completed her undergraduate studies in chemistry at The College of New Jersey in 2007, performing research with Professor David A. Hunt. Upon graduation, Emily worked at PTC Therapeutics, then located in South Plainfield, NJ, for several months before joining Bristol Myers Squibb in 2008 where she supported the discovery of new medicines to treat metabolic diseases. In 2009, Emily returned to academics to obtain her Ph.D. degree under the supervision of Phil S. Baran at Scripps Research in La Jolla, CA. Her graduate research focused on unified approaches to the total synthesis of deterpenoid and related diterpenoid alkaloid natural products.
In 2014, Emily moved back to the east coast to re-join Bristol Myers Squibb (BMS) within the Oncology Discovery Chemistry department in Princeton, NJ. She has participated in or co-led teams that have identified multiple clinical candidates for cancer immunotherapy. In 2019, she began supporting the first targeted protein degradation programs at BMS and has since taken on increasing responsibility in leading and shaping the strategy of the BMS induced proximity platform to support the discovery of ligand-directed degraders (LDDs), molecular glue degraders (e.g. CELMoDsTM), and other induced proximity approaches beyond degradation. She is listed as an inventor on >20 published patents and patent applications and is a co-author on >20 publications. For this work, she has been recognized with the 2022 ACS DOC Industrial Early Career Investigator Award and the 2026 ACS WCC Rising Star Award.