Dina Lyon
About Dina Lyon
Dina Lyon is a Clinical Study/Trial Manager specializing in Clinical Research Operations and Regulatory Affairs, currently working at the National Institutes of Health. With over 20 years of experience in medical countermeasures development and regulatory affairs, she has held various roles in prominent organizations, including the Henry M. Jackson Foundation and the U.S. Department of Veterans Affairs.
Current Role at National Institutes of Health
Dina Lyon serves as a Clinical Study/Trial Manager in Clinical Research Operations and Regulatory Affairs at the National Institutes of Health (NIH). She has been in this role since 2023. In her position, she is responsible for overseeing clinical studies and ensuring compliance with regulatory standards. Her work involves managing the operational aspects of clinical trials and contributing to the advancement of medical research.
Previous Experience at The Henry M. Jackson Foundation
Dina Lyon held multiple roles at The Henry M. Jackson Foundation for the Advancement of Military Medicine. From 2011 to 2018, she worked as a Clinical Research Manager and RN, contributing to projects at Walter Reed National Military Medical Center and the Uniformed Services University. She later served as a Senior Clinical Research Project Manager and Health Policy Analyst from 2020 to 2021, focusing on the Air Force Research Laboratory. Additionally, she worked as a Regulatory Research Scientist and Health Policy Analyst from 2018 to 2021 in the Air Force Office of Scientific Research.
Educational Background and Ongoing Studies
Dina Lyon has a robust educational background. She is currently pursuing a Master of Science in Bioinformatics at The Johns Hopkins University, expected to be completed in 2024. She previously earned a Master of Science in Biotechnology from the same institution. Additionally, she holds a Bachelor of Arts in Natural Sciences & Mathematics from Thomas Edison State University and a Bachelor of Science in Nursing from George Mason University. She also completed a Graduate Certificate in Executive Management from the University of Notre Dame.
Experience in Clinical Research and Medical Device Development
Dina Lyon has over 20 years of experience in preclinical and medical countermeasures development through clinical trials across various sectors, including industry and federal agencies. She has extensive expertise in medical device development, particularly in the DeNovo and 510k processes. Her background includes over 10 years of experience in FDA regulatory and health policy analysis, focusing on medical products such as devices, biologics, and drugs.
Military and Regulatory Affairs Experience
Dina Lyon's career includes significant experience within the military and regulatory affairs. She served as a Biomedical Research Manager and Active Duty Staff Sergeant in the U.S. Army from 2000 to 2009. This military background provides her with a unique perspective on the medical and technological needs of the military. She has facilitated scientific programs within the Department of Defense and Veterans Affairs, leveraging her expertise as a regulatory scientist and strategist.