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Dr. William E. Gannon, Jr., has served as Medical Director and Regulatory Affairs Advisor to Curemark since 2008. His responsibilities include oversight of the clinical and regulatory functions of Curemark’s clinical operations, including medical monitoring and clinical protocol design.

Dr. Gannon’s clinical trial experience covers a range of therapeutic areas, medical devices and biologic categories. Over the past 27 years, he has designed and led over 50 Phase I through Phase IV clinical trials around the world.

Dr. Gannon holds a Masters in Business Administration from George Washington University in Washington, DC, a Doctor of Medicine (M.D.) degree from Ross University/Case Western Reserve University and a Bachelor of Arts from The Catholic University of America in Washington, DC.