Mary Ann F Wojcik, MS, ELS, MWC, is an accomplished regulatory and medical writer with extensive experience in the pharmaceutical industry. Currently serving as an Expert Regulatory Writer and Expert Medical Writer at Novartis since May 2010, Mary Ann has contributed significantly to various pivotal submissions, including clinical study reports and risk management plans. Previously, at sanofi-aventis from April 2003 to April 2010, Mary Ann worked as a Regulatory Clinical Medical Writing Consultant, producing essential documents such as protocols and regulatory letters. Mary Ann’s career began at Johnson & Johnson, where roles included Director of Electronic Document Management and Assistant Director Medical Writing, overseeing document management and writing functions for various gastrointestinal therapeutics. Mary Ann's expertise is further established through earlier work at Covance as a Senior Medical Writer. Mary Ann holds a Master of Science in Human Biochemistry from the College of Dental Medicine at Fairleigh Dickinson University.
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