Ann O'Heney

Ann O'Heney is a seasoned professional in the pharmaceutical industry, currently serving as Senior Director, R&D IT - Global Clinical Lead and Senior Director, R&D Regulatory IT at Teva Pharmaceuticals since August 2016. O'Heney has extensive experience in regulatory operations, having previously worked as a Regulatory Operations Consultant from September 2015 to August 2016. Prior to that, O'Heney spent several years at Merck, holding positions such as Director of Regulatory Information Management and Director of Regulatory Content Submission Management, where responsibilities included leading multifaceted teams and overseeing strategic projects in global submission processes. O'Heney's career also included significant roles at Merck/Schering-Plough Research Institute, with expertise in regulatory submissions and process improvement initiatives. O'Heney holds a BA in Anthropology from Mount Holyoke College and a Programming Certificate from Chubb Institute for Computer Technology.