Keith Weber

Keith Weber is an experienced professional in regulatory submissions and project management, currently serving as a Director at Merck since November 2015, where responsibilities include leading the production of high-quality submission assemblies, training staff, and ensuring compliance with submission guidelines. Prior to this role, Weber worked at LIQUENT as a Senior Regulatory Associate, leading project teams in regulatory service delivery. Additional experience includes roles at Roche Pharmaceuticals, managing electronic and paper submissions, and serving as a liaison for DDMAC submissions. Keith Weber holds a Master of Business Administration from Caldwell University, RAC certification from RAPS, and a Certified Project Manager designation, combining academic credentials with a robust background in regulatory affairs.