Dina Lyon

Background

About Dina Lyon

Summated experience: In all positions: removes barriers to performance, deconstructs silos, pulls together high performing teams, & breaks through the "never been done before" line items >20 yrs spanning preclinical/medical research & development through medical device, drug, & biologic trials spanning industry, federal agencies, academia, & nonprofits > 15 yrs in neurodegenerative disease/traumatic brain injury/neurosensory/olfactory impairment >10 yrs medical device development within industry & the DoD (DeNovo, 510k)>10 yrs dedicated to FDA/regulatory & health policy analysis, intelligence, & strategy largely focused on clinical stage medical products (med devices, biologics, drugs, etc.)>10 yrs drafting regulatory/health policy, producing high impact technical documents, and briefing/providing recommendations to senior scientific & operational executive leaders I bring conscientiousness, critical analysis, and dogged dedication to my professional setting. My experience and education allows for a wide array of application and ability in clinical research and regulatory science. My years in the Army and my time with the DoD have allotted me a unique perspective on the medical and technological needs of the military, and my special interest and training in biotechnology allows me a unique perspective on potential diagnostic and therapeutic applications. My clinical operations experience allows for propulsion of any clinical trial program, and my experience and training as a regulatory scientist & strategist has led to tangible gains in facilitating scientific programs within the DoD, VA, & NIH. I've also been successful in reducing spending to potentiate more efficient and effective programs, resulting in 7-digit(+) savings on 10-digit portfolios.