Amy Porter is a Senior Counsel in Clinical R&D at AbbVie, where they advise on global research activities throughout the phases of clinical development and develop patient informed consent forms. Previously, at Eli Lilly and Company, they served in various roles, including Consultant in Regulatory Intelligence and Associate Consultant focusing on neuroscience opportunities. They also held positions at Elanco as a Legal Consultant, where they managed contracts for R&D and collaborated on business development transactions. Amy earned a JD from Indiana University Robert H. McKinney School of Law, an MS in Molecular Biology from Ball State University, and a BS in Biology from Indiana University–Purdue University Indianapolis.
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