Lori Canney is currently the Associate Director of Clinical Operations at Merck, where they oversee clinical studies and ensure project delivery within timelines and budgets. With extensive experience in clinical trial management throughout both small biotech and large pharmaceutical environments, Lori has worked in various capacities including Clinical Project Manager and Clinical Protocol Manager. Having begun their career as a Medical Research Associate at Boehringer Ingelheim Pharmaceuticals, Lori's expertise spans the complete clinical development process from Phase I to IV. Lori is pursuing a Bachelor of Arts in Psychology at Western Connecticut State University.
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