Ruth Lowth

Ruth Lowth is a Senior Regulatory Project Manager at AbbVie, where they have worked since 2016, specializing in regulatory affairs for clinical trial applications and marketing authorization across various therapeutic areas. Ruth's extensive experience in the field began in 2000 at AstraZeneca and includes roles at prestigious companies such as Allergan Pharmaceuticals and ICON plc. They hold a BSc in Chemistry from Bangor University and a Post Graduate Diploma in Regulatory Affairs from the University of Wales, Cardiff, which they completed with distinction. Ruth is adept at communicating and collaborating with cross-disciplinary teams while managing multiple projects under tight deadlines.