Erica Behnke Pharm.D, M.S. is a highly skilled professional with extensive experience in regulatory affairs and pharmaceutical project management. Currently serving as a Labeling Manager at Bristol Myers Squibb since March 2018, Erica Behnke proactively prepares and supports electronic Common Technical Document (eCTD) submissions while ensuring compliance with global regulatory requirements. Previous experience includes a role in Regulatory Affairs at Cognizant and an internship in Pharma Development Project Management at Daiichi Sankyo, where Erica Behnke contributed to tracking clinical trials and managing expenditures. Additional roles encompass research assistance at VA New Jersey Health Care Hospital, recruiting at Planned Companies, and service as a Corporal in the United States Marine Corps. Academically, Erica Behnke holds a Doctor of Pharmacy (Pharm.D.) and a Master of Science in Pharmaceutical Chemistry from Fairleigh Dickinson University.
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