Susan Greenbaum

Susan Greenbaum serves as Principal Clinical Controls Manager at Stryker since March 2019, focusing on compliance with FDA regulations and international guidelines. In addition, Susan is the VP of Clinical, Regulatory and Quality at GDCI Consulting, Inc. since February 2002, providing comprehensive clinical research services for the biotechnology and pharmaceutical sectors. Previous roles include Director of Regulatory and Quality at BioCure (2008-2009), where substantial contributions were made to the clinical trial and regulatory submission processes for biotechnology products, and Regulatory Affairs Specialist II at Inamed, supporting human bioengineered collagen products. Early career experience includes serving as Regulatory Affairs Associate at Medtronic. Susan earned a B.A. in Environmental Studies from Florida International University between 1996 and 1998.