David Rivera, M.S., is an accomplished regulatory affairs professional with extensive experience in the pharmaceutical industry. Currently serving as Senior Manager of Regulatory Affairs at Edenbridge Pharmaceuticals, LLC since May 2018, David has held various roles in regulatory affairs, including positions at Teva Pharmaceuticals and Actavis plc (now Allergan). David's career began at Teva Pharmaceuticals as an Associate I and included a role as a Clinical Validation Specialist at Dendreon. David holds a Master's degree in Regulatory Affairs from the University of Maryland and a Bachelor of Science in Integrated Science, Business, and Technology from La Salle University.
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