Megan Lamberti
Vice President of Clinical and Regulatory Affairs
Nilo Medical Consulting Group
Megan Lamberti has over 10 years of experience in clinical and regulatory affairs for the development and introduction of novel medical devices, in vitro diagnostics and pharmaceutical products. She began her career working on low-cost medical devices for resource scarce healthcare environments. She worked as an engineer and transitioned to managing clinical and regulatory affairs for a start-up company developing diagnostic and monitoring equipment for the intensive care unit. Since 2018, Ms. Lamberti has worked as a consultant specializing in clinical trial design and execution and regulatory affairs, including medical writing services. Megan has worked as a clinical research associate (CRA), monitor and project director on the CRO side of research, in industry, managing clinical affairs on behalf of her clients, and in academia as a clinical research coordinator, which has yielded her cross-functional skill sets in the conduct of clinical research.