Mark Welsh

Mark Welsh is currently a Regulatory Affairs Consultant/Manager at Genpact, where they analyze CMC submission events and ensure compliance with regulatory milestones. Previously, Mark held various roles, including Senior Data Manager at Ockham and Pharmacovigilance Officer at Chiltern International, where they managed project timelines for clinical trials. Their experience spans several positions in data management and clinical data coordination, including leadership roles at Phastar and Quintiles. Mark earned valuable expertise in managing phase II–IV clinical trials and liaising with regulatory teams throughout their career.