Burke Byrne

Burke Byrne has a significant amount of work experience in the regulatory affairs field. Burke served as the Manager of Regulatory and Clinical Affairs at Lipocine Inc. starting in December 2014. Prior to that, they worked at Watson Laboratories as the Manager of Regulatory Affairs from July 2008 to December 2014. During this time, they successfully managed multiple large regulatory projects and negotiated with FDA and other health authorities. Before their manager role, Burke worked as an Associate at Watson Laboratories from February 2005 to July 2008. In this position, they were responsible for various tasks such as crafting briefing packages, writing regulatory documents, and managing drug marketing applications. Additionally, Burke Byrne served as a Project Coordinator at Watson Laboratories from November 2002 to February 2005. In this role, they managed successful product launches, supervised equipment acquisitions, and implemented a resource management program.

Burke Byrne's education history includes obtaining a Bachelor of Science (B.S.) degree in Biology, General from the University of Utah. Additionally, they pursued a Master of Business Administration (M.B.A.) degree from the University of Utah - David Eccles School of Business. Specific start and end years for each educational experience are not provided.