Kimberly Lamberti, PhD

SENIOR CLINICAL & REGULATORY AFFAIRS SPECIALIST II

Dr. Kimberly Lamberti has been working in medical device development since 2017, across a breadth of industry and academic settings. She holds dual degrees in Mechanical and Biomedical Engineering from Carnegie Mellon University, where she built a foundation in engineering principles and developed a passion for healthcare innovation. Dr. Lamberti went on to earn her PhD in Medical Engineering and Medical Physics from the joint Harvard-MIT Health Sciences and Technology program. Her dissertation, conducted in close collaboration with industry partners, focused on enhancing the clinical utility of cardiovascular support devices. Her work integrated benchtop, preclinical, and clinical research to advance mechanistic understanding of the human-device interface and its effects on native physiology.

In parallel to her academic training, Kim gained hands-on industry experience in early-stage medical device and biotech companies, leading projects in R&D and new product development. She also served as a Venture Creation Fellow at a life sciences–focused venture capital firm, where she ideated and pitched novel company concepts. Additionally, she has provided consulting in clinical and regulatory affairs, helping bring both medical devices and pharmaceutical products to market since 2019.

She brings all of these skills and experiences to her role at NMCG, including her interdisciplinary engineering and clinical training, and expertise in medical and technical writing, data analysis, and study design and strategy, to support clients in advancing their technologies to the clinic. 

For more information, please see her LinkedIn Profile.