Victoria Dormer

Victoria Dormer is an experienced professional in regulatory affairs and project leadership within the clinical study sector. Currently serving as the TMF Project Leader at CE3 Inc. since August 2013, Victoria is accountable for the management and delivery of electronic Trial Master File (eTMF) services, overseeing all operational aspects of clinical studies. Previous roles include Regulatory Specialist positions at Durata Therapeutics and Boehringer Ingelheim, where Victoria contributed to inspection readiness, regulatory submissions, and lifecycle maintenance of products. Victoria demonstrates strong leadership capabilities, effective communication skills, and a solid understanding of compliance and regulatory processes, supported by a background in managing teams and complex projects. Victoria is pursuing a Bachelor's Degree in Health Science from Kaplan University.