ÂÜÀòÂÒÂ×

Madison Adams is a seasoned professional in regulatory affairs with significant experience in the pharmaceutical industry. Currently serving as Senior Manager, Regulatory Affairs at Kymera Therapeutics since December 2020, Madison has previously held roles such as Regulatory Affairs Manager and Pre-Clinical Study Manager. Prior to joining Kymera Therapeutics, Madison worked at Enanta Pharmaceuticals from March 2018 to December 2020, holding positions including Bioanalytical Quality Control Specialist and Associate Scientist, as well as an intern role at the DMPK Lab. Madison's career began with an internship in the Quality Control Lab at BSP Pharmaceuticals S.p.A. in 2017. Madison holds a Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices from Northeastern University and a Bachelor of Science in Pharmaceutical Sciences from the University of Rhode Island.