Doreen is a clinical trial professional with over 30 years of extensive experience in all aspects of the Research and Development industry, including study management in multiple therapeutic/study phase areas. She has worked on Phase I – III clinical trials from inception to completion. Her core strengths include clinical trial planning and oversight, regulatory requirements/FDA audits, clinical data analysis, TMF, and risk based monitoring operations. Aside from work, she loves to garden, read historical fiction books, volunteer and this summer she checked off one of her bucket list goals; she was able to see the Northern Lights from her house in CT due to a ‘solar storm’.