Clinical Trial Podcast | Conversations with Clinical Research Experts

How Statisticians Really Think About Endpoints, Power, and FDA Review with Roseann White

Statistics influence almost every major decision in a clinical trial. In this episode, Roseann White, a retired biostatistician with more than 30 years of experience, j

How Clinical Research Hiring Decisions Are Actually Made with Giovanni Lauricella

Why do qualified candidates apply to role after role in clinical research and never hear back? In this episode of the Clinical Trial Podcast, we unpack what's really ha

Designing and Conducting Observational Studies with Thomas Newman, MD, MPH

What separates strong clinical research from misleading conclusions? Often, it comes down to study design. In this episode of the Clinical Trial Podcast, Kunal Sampat

Cardiovascular Device Development: From Idea to Reality

Bringing a high-risk cardiovascular device from concept to patient care requires more than innovation - it requires carefully designed clinical trials, strong operational

Best Practices for Clinical Trial Budgeting

Clinical trial budgeting remains one of the biggest bottlenecks in study startups, driving delays, rework, and frustration across sponsors, CROs, and research sites. In

Risk Based Monitoring in Clinical Trials with Artem Andrianov

Risk-based monitoring has been discussed in clinical research for more than a decade, yet many organizations still struggle to implement it in a meaningful and effective

Leading a Clinical Research Organization in the European Union with Dr. Philip Raeth

In this episode of the Clinical Trial Podcast, host Kunal Sampat sits down with Dr. Philip Räth, Managing Director of Palleos Healthcare, to discuss leading Clinical Rese

Sponsor, Site, and Technology Vendor Collaboration with Mike Wenger

To get more insights about clinical research technology from a vendor's perspective, I invited Mike Wenger on the Clinical Trial Podcast. Mike Wenger is a software deve

Inspection Readiness with Donna Dorozinsky

To discuss what inspection readiness entails, I invited Donna Dorozinsky, Founder & CEO of Just in Time GCP to the show.   Donna is a business consultant who has over 30

Clinical Trials in Saudi Arabia with Dr. Majed Al Jeraisy

Saudi Arabia's modern healthcare system, diverse patient population, and research-savvy healthcare professionals make it a great place to conduct clinical trials. To lear

Cardiology Clinical Trials with Dr. Gregg Stone

To learn more about this important field of cardiovascular clinical research, I invited Dr. Gregg Stone on the podcast. Dr. Stone is an Interventional Cardiologist and

Clinical Trial Insurance with Dan Fuld

In this episode, you will learn about what type of insurance (if any) is needed to conduct a clinical trial. We also discuss different insurance provisions, choosing the

Diabetes Clinical Trials with Dr. Stayce Beck

To learn more about clinical trials in diabetes, I invited Dr. Stayce Beck, Global Vice President of Clinical Affairs at Dexcom Inc. on the podcast.  Dr. Beck currently

Access to Novel Medical Products with Dr. Alison Bateman-House

Providing patients access to novel medical products can be challenging to navigate for sponsors and trial participants alike.  To learn more about expanded access, comp

Clinical Research as a Profession with Erika Stevens

Unlike an electrical engineer or a plumber, clinical research roles are not explicitly defined or categorized as such, in government employment databases. There are no

Community Engagement in Clinical Trials with Chris Komelasky

To learn about community engagement in clinical trials, what it means, recent regulations and guidance documents, I invited Chris Komelasky, CEO and Co-founder of SiteBri

Community health system-based research with JoAnne Levy

Community health system-based research continues to become an important focus area for pharmaceutical and medical device sponsors given the recent FDA guidance on diversi

Postmarket Surveillance Studies with David Rutledge

In this episode, we're going to talk about Postmarket Surveillance Studies.  In light of the EU Medical Device Regulation (MDR), medical device manufacturers are requir

Human-centered design role in clinical trials with Bruce Hellman and Ben James

In this episode, we explore the role of design in clinical trials. Most clinical research professionals are so focused on protocol design, data collection, and analysis

Clinical Trial Site Networks with Christian Burns

There are advantages and disadvantages when it comes to being a standalone clinical trial site.  Standalone clinical trial sites enjoy the freedom of running their own