Christine Granfield

Christine Granfield has extensive work experience in regulatory affairs, specifically in the healthcare and medical device industry. Their most recent role is Vice President of Regulatory Affairs & Quality at Leap Therapeutics since August 2020. Prior to that, they worked as an Independent Consultant in Regulatory Affairs at Granfield Associates, LLC from October 2016 to August 2020. Christine also served as the Senior Director of Regulatory Affairs at Genzyme from October 1998 to June 2011 and as a Project Manager in Regulatory Affairs at Boston Scientific from 1994 to 1998. Christine Granfield started their career as a Regulatory Engineer at B. Braun Medical from 1992 to 1994. Christine also has experience working as a Biomedical Engineer in the Office of Device Evaluation at the FDA from 1990 to 1992.

Christine Granfield obtained a Bachelor of Science in Engineering in Biomedical Engineering from The Catholic University of America from 1986 to 1990.