Kimberly Lamberti, PhD
Senior Clinical and Regulatory Affairs Specialist II
Nilo Medical Consulting Group
Kim Lamberti, PhD, is a clinical and regulatory affairs consultant, specializing in clinical trial design, medical writing, and clinical trial operations for medical devices and combination products. In her current role as a Senior Clinical and Regulatory Affairs Specialist II at Nilo Medical Consulting Group, she supports decentralized and traditional clinical trials, leads preparation of regulatory documentation, and advises Sponsors on clinical evidence generation for early- and mid-stage technologies. Dr. Lamberti earned her PhD in Medical Engineering and Medical Physics from the Harvard-MIT Program in Health Sciences and Technology, where she conducted bench, preclinical, and clinical studies focused on improving medical device performance and physiologic assessment. She has authored five peer-reviewed publications and delivered six scientific presentations across national and international forums. Her work has been recognized through multiple honors, including the NIH F31 Fellowship, the NSF Graduate Research Fellowship, and multiple presentation awards.