Richard Peck

Dr. Peck has over 30 years’ experience as a clinical pharmacologist with Glaxo Wellcome, Eli Lilly and Roche. His group at Hoffmann-La Roche defines dosing and explores response variability for small and large molecules throughout development, regulatory approval and subsequent clinical use. His current research focus is to develop ways to identify precision dosing algorithms in early clinical development that could be tested in pivotal pre-approval clinical trials, thereby enabling precision dosing to be integral to approval for new drugs. He earned his medical degree at St. John’s College, Cambridge University and worked for several years as a hospital physician before embarking on a career in clinical pharmacology.