Lisa A.

Lisa A. has over 20 years of experience in various roles in the pharmaceutical industry. Lisa is currently the VP of Global Clinical Regulatory Affairs and Quality at Sana Biotechnology, Inc. Lisa previously held positions as VP of Regulatory and Clinical Quality at Nkarta Therapeutics, Inc., Sr Director of Regulatory Affairs and Quality Assurance at REVOLUTION Medicines, and Director of Regulatory Affairs at Medivation. Lisa also has experience at Genentech, where they were an Associate Regulatory Program Director, Development Project Manager, Manager of Clinical Supply Chain, and CMC Project Manager. Prior to that, they worked at Pfizer as a Quality Assurance Manager and QA Specialist, and at Abbott Laboratories as a Process Engineer.

Lisa A. holds a Professional Certificate in Clinical Research Conduct and Management from UC Berkeley Extension, which they obtained from 2007 to 2009. Prior to that, from 2000 to 2002, they earned a Master of Science degree in Quality Assurance & Regulatory Affairs from Temple University. Lisa also holds a Bachelor of Science degree in Chemical Engineering from Iowa State University, obtained from 1993 to 1995, and a Bachelor of Science degree in Biochemistry from the University of Iowa, which they completed from 1982 to 1986.