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Stuart Cotter

Vice President of Product Management, Advarra

Stuart Cotter is the Vice President of Product Management at Advarra. In this role, he collaborates with current customers and the research community to understand their challenges and translates those challenges into solution-based enhancements to our product offerings. Cotter also leads the Advarra Site-Sponsor Consortium, helping to seamlessly connect site and sponsor technology by addressing key data and process inefficiencies across the clinical research ecosystem. Prior to joining our product management team, Cotter worked as a Product Support Specialist on Allegro CTMS, where he worked alongside dozens of small- to mid-sized research sites to help them overcome their operational hurdles.

Stuart Cotter

Latest Posts by Stuart

 
Webinar

Bridging the Gap: A Standardized Approach to Clinical Trial Document Management

Representatives from the Advarra Site-Sponsor Consortium will discuss a standards-based integration and automation of research technology.

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Blog

Beginner’s Guide to eTMF, eISF, and Regulatory Research Documents

Global & FDA regulations dictate how researchers organize & store trial documents. Learn the basics of eTMF & eISF clinical research tools

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5 min. read
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Blog

Best Practices in Pre-Screening Includes Use of Technology

Explore the benefits of pre-screening potential participants before they move on to the informed consent process.

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6 min. read
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Blog

It’s Time for Sites to “Bring Your Own Technology” (BYOT)

The Bring Your Own Technology philosophy will produce synchronization between sites & sponsors, which improves both care & clinical outcomes.

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4 min. read
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Blog

How to Be Research Ready: Today and Beyond

If presented with a new study, are you prepared to take it on? Efficient study activation can set the pace for a successful clinical trial.

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3 min. read
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Blog

Building Remote Workflows within eRegulatory Document Management: Subject Binders & SOPs

Advarra eRegulatory Management System now supports the storage and remote monitoring of Subject Binders and SOPs, increasing compliance, and centralizing your study documents.

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3 min. read
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Blog

4 Reasons Your Institution Needs an eRegulatory System

Using physical binders or an internal shared drive can slow research operations. Implementing an eRegulatory system helps institutions streamline research by transforming key workflows.

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3 min. read
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Blog

Q&A – Regulatory Fine Points: Exploring 21 CFR Part 11 Validation

Advarra's experts answer audience questions from our Regulatory Fine Points: Exploring 21 CFR Part 11 Validation webinar.

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5 min. read
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Webinar

Creating an Integrated Approach to Regulatory Management at Your Institution

Over the past year, clinical research professionals have faced unprecedented challenges related to both the clinical and operational management of their research. Maintaining regulatory compliance and visibility within an increasingly remote environment has been a key focus area for many institutions.

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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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