Jill Schweiger is a highly qualified and accomplished leader with a highly demonstrable track record of success in the areas of clinical studies and regulatory affairs. She has previously served as a Vice President and Director in at least six early stage medical device companies, as well as multinational med tech organizations such as Baxter Healthcare Corporation and Eli Lilly & Company.
Most recently, Schweiger served as Vice President, Clinical Studies & Regulatory Affairs for Flowonix Medical, Inc., a company focused on the development of implantable infusion pumps designed to deliver therapeutic drugs to relieve a variety of chronic disorders, such as spasticity and chronic intractable pain. While there, she was responsible for the development and execution of US and European regulatory and clinical strategies, that achieved PMA Approval in the US and CE Mark in Europe.
Prior to that, she was Vice President, Clinical & Regulatory Affairs at Angel Medical Systems, Inc., a company specializing in the development of an implantable cardiovascular monitoring system designed to detect ischemia which could be indicative of a heart attack. While there, she was responsible for developing and executing regulatory, clinical and quality strategies to support business and financing objectives and U.S. and international marketing applications.