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AI promises to revolutionize clinical trials and reshape regulatory oversight. But is the pharma industry ready? And can the FDA keep pace with the technology?

In this episode of the HealthBiz Podcast, host David Williams is joined by Tom Doyle, Chief Technology Officer of Medidata, to discuss the promises and potential pitfalls of AI in clinical trials.


🎙️⚕️ABOUT TOM DOYLE
Tom Doyle heads product development at Medidata, a leader in clinical research technology and a life sciences arm of Dassault Systèmes. In this role, Tom leads Medidata’s work in developing industry-leading solutions for patients, sites, sponsors, and CROs, improving and accelerating the design, execution, and oversight of clinical trials – essential in bringing new and novel treatments for patients.

Tom joined Medidata in 2019, bringing 20 years of global experience in medtech and data science. Before coming to Medidata, Tom held leadership roles at Janssen and at Boehringer Ingelheim, championing technology to drive new experiences and better insights. He’s passionate about the power of innovation to transform clinical research towards better outcomes and better experiences for patients.

Tom has a BMath in computer science from the University of Waterloo in Ontario, Canada.


🎙️⚕️ABOUT HEALTH BIZ PODCAST
HealthBiz is a CareTalk podcast that delivers in-depth interviews on healthcare business, technology, and policy with entrepreneurs and CEOs. Host David E. Williams — president of the healthcare strategy consulting boutique Health Business Group — is also a board member, investor in private healthcare companies, and author of the Health Business Blog. Known for his strategic insights and sharp humor, David offers a refreshing break from the usual healthcare industry BS.

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