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Software Solutions for Clinical Research Sites with Ryan Jones

Clinical Trial Podcast | Conversations with Clinical Research Experts

Release Date: 11/23/2021

Clinical Trials in Saudi Arabia with Dr. Majed Al Jeraisy show art Clinical Trials in Saudi Arabia with Dr. Majed Al Jeraisy

Clinical Trial Podcast | Conversations with Clinical Research Experts

Saudi Arabia’s modern healthcare system, diverse patient population, and research-savvy healthcare professionals make it a great place to conduct clinical trials. To learn more about the clinical trial requirements in Saudi Arabia, I invited Professor Majed Al Jeraisy on the show.   Dr. Al Jeraisy is an Associate Professor of Pharmacy Practice, College of Pharmacy, King Saud Ben Abdulaziz University for Health Sciences and Pediatric Clinical Pharmacy Consultant in King Abdullah Specialized Children Hospital. He was appointed as the chairman of the research office at King Abdullah...

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Cardiology Clinical Trials with Dr. Gregg Stone show art Cardiology Clinical Trials with Dr. Gregg Stone

Clinical Trial Podcast | Conversations with Clinical Research Experts

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 Director of Academic Affairs for the Mount Sinai Heart Health System and Professor of Medicine (Cardiology) and Professor of Population Health Sciences and Policy at the Icahn School of Medicine at Mount Sinai in New York, NY.  He has served as the national or international principal investigator for more than 150 national and international multicenter randomized trials and studies (many of which have led to new device...

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Clinical Trial Insurance with Dan Fuld show art Clinical Trial Insurance with Dan Fuld

Clinical Trial Podcast | Conversations with Clinical Research Experts

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 right insurance partner, regulatory requirements that dictate insurance and much more. Dan is a seasoned insurance professional with 10+ years of underwriting and broking experience. Dan and his team also assist in the implementation of alternative risk mitigation strategies, and see themselves as strategic partners to those in the life science space. Dan graduated from the Katie School of Insurance at Illinois State...

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Diabetes Clinical Trials with Dr. Stayce Beck show art Diabetes Clinical Trials with Dr. Stayce Beck

Clinical Trial Podcast | Conversations with Clinical Research Experts

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 oversees clinical operations, clinical strategy and science, biometrics and human factors at Dexcom Inc, a leading manufacturer of continuous glucose monitors (CGMs) Prior to joining Dexcom, Dr. Beck worked at Food and Drug Administration for over ten years, spending time as a scientific and regulatory reviewer, a chief of the Diabetes Diagnostic Devices Branch, and Deputy Office Director of Personalized Medicine and...

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

Clinical Trial Podcast | Conversations with Clinical Research Experts

Providing patients access to novel medical products can be challenging to navigate for sponsors and trial participants alike.  To learn more about expanded access, compassionate use, Right to Try laws, I invited Dr. Alison​ ​Bateman​-​House​, ​PhD​, ​MPH, MA​, ​an​ ​Assistant​ ​Professor​ ​in​ ​the​ ​Division​ ​of​ ​Medical Ethics​ ​at​ ​NYU​ ​Grossman​ ​School​ ​of​ ​Medicine​.  Dr. ​Bateman​-​House​ ​is​ ​co​-​chair ​of​ ​the​ ​Working​ ​Group​ ​on Compassionate​...

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Clinical Research as a Profession with Erika Stevens show art Clinical Research as a Profession with Erika Stevens

Clinical Trial Podcast | Conversations with Clinical Research Experts

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 certification or degree requirements to work as a clinical research professional either. To explore the topic of clinical research as a profession, I invited Erike Stevens on the podcast. Erika advises life sciences, academic medical centers, hospitals, cancer centers, foundations and health systems process improvement initiatives for productivity, quality and efficiency in operations, cross-functional relationships,...

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Community Engagement in Clinical Trials with Chris Komelasky show art Community Engagement in Clinical Trials with Chris Komelasky

Clinical Trial Podcast | Conversations with Clinical Research Experts

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 SiteBridge Research, on the podcast.  SiteBridge Research is an Integrated Research Organization (IRO). Chris and his team help connect physicians and their patients to clinical trials and facilitate the process by reducing barriers for sites and participants. Prior to the launch of SiteBridge, Chris has held various leadership roles at PPD, GlaxoSmithKline, Accenture and ZS Associates. Chris holds a B.S. in Systems Engineering...

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Community health system-based research with JoAnne Levy show art Community health system-based research with JoAnne Levy

Clinical Trial Podcast | Conversations with Clinical Research Experts

Community health system-based research continues to become an important focus area for pharmaceutical and medical device sponsors given the recent FDA guidance on diversity in clinical trials.  Our guest for this episode is JoAnne Levy, Vice President at Mercy Research, a part of Mercyhealth.  Mercy Research is one of the largest fully integrated, community health system-based research organizations in the United States with more than 40 acute care, managed, and specialty hospitals, convenient urgent care locations, imaging centers and pharmacies. In 2022, over 38,000 Mercy patients...

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Postmarket Surveillance Studies with David Rutledge show art Postmarket Surveillance Studies with David Rutledge

Clinical Trial Podcast | Conversations with Clinical Research Experts

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 required to implement a Postmarket Surveillance (PMS) plan, which in turn may require them to conduct Postmarket Surveillance Studies.  The importance of such studies has grown in recent years as regulators want to know about the safety and effectiveness during the lifetime of a medical device.  To learn about Postmarket Surveillance Studies regulatory requirements, process for collecting clinical data for such...

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

Clinical Trial Podcast | Conversations with Clinical Research Experts

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 that it’s easy to overlook the importance of well-designed technology that supports clinical trials. One such technology product is electronic Patient Reported Outcomes or ePROs. ePROs are surveys that are presented to and completed by clinical trial participants as part of the study requirements.  To learn more about ePROs and the role of design in clinical trials, I invited Bruce Hellman and Ben James on the Clinical...

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More Episodes

As the clinical research ecosystem becomes more site and patient centric, I was curious about what an ideal software stack looks like for clinical research sites.

It goes without saying you need a laptop and stable internet connection to do business in this day and age.

But what else do you need to keep yourself organized as a clinical research site? 

How can a clinical trial site bring most value to their research participants, run a profitable research operation, and not overwork employees with administrative tasks?

To answer these questions and more, I invited Ryan Jones to join me on the show. If this is your first time listening to Ryan, I also invite you to check out my earlier interview with Ryan, Solving Clinical Research Problems Using Technology, episode #12, of the show.

Aside from the technology discussion, I’m a huge fan of the company culture that Ryan and his leadership team at Florence Healthcare have created for their employees. We wrap up the episode with a couple of great book recommendations that you might be interested in reading.

I hope you enjoy my conversation with Ryan Jones.

Ryan Jones on LinkedIn and Twitter 

Florence Healthcare on LinkedIn and Twitter