About me
A seasoned professional with over 19 years of experience in the Contract Research Organization (CRO) and pharmaceutical industry. Demonstrated expertise in leading and managing clinical trials, with hand on experience from both site and industry perspectives. Proficiency in overseeing the full lifecycle of clinical studies including clinical, regulatory and start-up, and decentralized trials operations across various phases of research. Skilled in driving strategic process improvements, serving as regulatory subject matter expert for Decentralized Clinical Trials (DCT), and acting as a controlled document liaison. Currently focused on supporting site solutions, with a particular emphasis on site adoption of home health services.
