Dr. Jeff Kingsley Interview

In this interview with Dr. Jeffrey Kingsley, we talk about what it takes to start and manage a clinical trial site, the world of site networks, how an investigator can decide whether or not a clinical study is worth their time, volunteering for the Association of Clinical Research Professionals (ACRP), Food and Drug Administration (FDA) audits, books and a lot more.

Dr. Kingsley is the President and CEO; Institute for the Advancement of Clinical Trials DBA IACT Health and an owner of 11 clinical trial sites.

He is a Fellow at Association of Clinical Research Professionals. Dr. Kingsley graduated with a master’s in business administration from Emory University, a doctorate in osteopathic medicine from Philadelphia College of Osteopathic Medicine, a master’s in science, biochemistry and a bachelor’s of science, biology, chemistry, history, cultural anthropology from the University of Scranton.

Please join me in this value-packed interview with Dr. Jeffrey Kingsley.

This episode is brought to you by CBI Events.

The team at CBI has put together a Digital Therapeutics event in New York City on December 3-4, 2018. Topics range from strategies for new digital health projects to perspectives from the venture capital community on investment requirements for digital therapeutics.

Whether you’re a pioneer in this space or want to know just the right amount of information to get started, this event is going to value packed for you.

Some benefits from your participation in this event include:

  • Learning strategies on how to ensure data integrity
  • Understanding regulatory approaches to digital therapeutics and how to seamless approval in all regions
  • Finding out about payer approval requirements and uncovering changing business models
  • Collaborating with others on standard definitions and approaches to what constitutes a digital therapeutic
  • And much, much, more.

If you want to learn and network with others in the Digital Therapeutics space, you should attend the 2018 event in New York City on December 3-4, 2018. 

As a listener to this podcast, I’ve got an exclusive $500 discount to this event. When I mean exclusive, it really is exclusive. 

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Register today to get your exclusive $500 off your event ticket using the code CTP500. This offer is only available to the Clinical Trial Podcast listeners.

Selected links from the episode:

Dr. Jeff Kingsley on LinkedIn

IACT Health

Association of Clinical Research Professionals

Society of Clinical Research Sites

Wall Street Journal

Vistage: Executive Coaching Organization

Harvard Business Review

Scrib’d

Get abstract

Books mentioned:

The Ideal Team Player: How to Recognize and Cultivate The Three Essential Virtues by Patrick M. Lencioni

Draw to Win: A Crash Course on How to Lead, Sell, and Innovate With Your Visual Mind

People mentioned:

Steve Jobs

Seneca

Cato

Marcus Aurelius

Show notes:

  • plan for volatility when starting a clinical trial site from scratch [05:45]
  • we’re all responsible for ensuring the appropriate clinical research training [07:56]
  • be conscious of your expenses as a clinical trial site [09:41]
  • tools or processes starting your own sites [12:01]
  • the importance of getting yourself plugged into the industry [12:32]
  • joining a site network and why they are not all created equal [13:11]
  • the importance of differentiation and how sites are the most fragmented side of the research industry [15:34]
  • I actually got seven majors in my undergrad [17:42]
  • broaden your experience, the more you can see outside of the box [18:34]
  • Lessons learned as a union factory worker [20:30]
  • most critical skill in my opinion in research is the ability to gain that level of competence where you can think independently [22:50]
  • how to decide whether or not a clinical study is worth your time? [24:35]
  • how can somebody get involved with ACRP and why it’s important? [28:13]
  • ACRP certification [30:26]
  • you can get a job in the industry in an atypical fashion [33:04]
  • FDA audits [34:34]
  • should sponsors conduct investigator meetings and whether sites should charge for their time to participate in such meetings [37:47]
  • remote versus risk-based monitoring, what are the differences [41:54]
  • the future is risk-based monitoring [44:35]
  • Use CTMS to conduct clinical trials more effectively [45:57]
  • how do you go about finding a CTMS solution [47:24]
  • define what “superman” looks like [48:23]
  • objectify the subjective [49:48]
  • negotiating study budgets and using data to drive your conversation [52:32]
  • how can a site ensure that clinical data quality is top notch [58:34]
  • hire quality individuals, pay attention to their capacity and making sure they have the tools to be successful [1:00:46]
  • not being average and revolutionizing research [01:12:32]

 

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