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James Riddle, MCSE, CIP, CPIA, CRQM

SVP, Global Review Services, Advarra

With 25+ years’ experience providing support to the clinical research community, James Riddle helps sponsors, CROs, and research sites advance clinical research with a mission to improve human health. His expertise includes developing and operationalizing processes for maximum efficiency, client satisfaction, and participant protection; development and implementation of technology solutions; and efficient, compliant operation of large clinical research review programs. Prior to Advarra, Riddle held leadership roles at two major central IRBs and served as a senior leader within the research oversight office at the Fred Hutchinson Cancer Research Center. He is also a member of CTTI, NWABR, SASI, and PRIM&R.

James Riddle

Latest Posts by James

 
Webinar

Regulatory Fine Points: Exploring 21 CFR Part 11 Validation

FDA is placing an increased emphasis on compliance with 21 CFR Part 11. Institutions, health systems, IRB offices, private research clinics, and developers—to name a few—need to understand the basics of the regulation and how to comply.

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Blog

Is GDPR Coming to the US? CCPA and Its Impact on Research

New California regulations apply to companies who have information about CA residents regardless of where the company is located. Read more:

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5 min. read
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Webinar

From Reactive to Proactive: How to Evolve Your Research Program During a Global Crisis

August 5, 2020

Many research programs are evaluating how to keep research moving forward in the face of critical staff shortages and budget limitations—during the COVID-19 pandemic and beyond. Sites are busier than ...

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Virtual Event

Virtual Symposium: Gene Therapy Research in the Age of COVID-19

June 5, 2020

Gene therapy research is expanding rapidly in the clinical setting, especially in oncology, rare diseases, and infectious diseases—in fact, gene therapy research plays a crucial role in responding to the ...

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Blog

Beyond the Regulations: More Considerations for Emergency Research

Go beyond the regulatory requirements and examine three key actions research organizations must consider before conducting planned emergency research.

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7 min. read
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Blog

A Tale of Two Sites: The Power of Integrated Research Administration

Learn how institutions attract more studies from the the tale of two sites: one with an integrated research administration, and one without.

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5 min. read
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