Esperion Therapeutics
Jo Ann Wells is an experienced professional in clinical quality assurance with a comprehensive background in the bio-pharmaceutical industry. Currently serving as the Director of Clinical Quality Assurance at Esperion Therapeutics since January 2016, Jo Ann previously operated as an Independent Consultant through JoAnn Wells Compliance Consulting, providing GCP consulting services from August 2013 to January 2016. Additionally, Jo Ann held the position of Center of Excellence Subject Matter Lead for Quality at YourEncore, contributing to technical content development for client proposals. Prior experiences include serving as the Director at Aastrom Biosciences, overseeing GCP and GMP compliance, and holding the role of Director of Clinical Quality Assurance at Pfizer from 1990 to 2007. Jo Ann's educational background includes a degree from Wayne State University.
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Esperion Therapeutics
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Through scientific and clinical excellence, and a deep understanding of cholesterol biology, the experienced Lipid Management Team at ESPERION is committed to developing new LDL-C lowering medicines that will make a substantial impact on reducing global cardiovascular disease, the leading cause of death around the world.