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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.

Latest Posts by Stuart

Webinar

Re-air: Not if, but When: A Study Manager’s Guide to Adaptability and Incoming Trends

Upcoming: May 9

Dive deeper into achieving critical milestones across study startup, conduct, and close out that every project manager should optimize.

Webinar

Not if, but When: A Study Manager’s Guide to Adaptability and Incoming Trends

Upcoming: May 2

Dive into achieving critical milestones across study startup, conduct, and close out that every project manager should optimize.

Blog

Checklist to Reduce Burden on Sites and Patients

Review a list of considerations for site-sponsor tasks to streamline startup, reduce redundancy, and refine technology choices for effective partnerships.

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5 min. read

Webinar

Sponsors: Are Your Sites Ready for an FDA Inspection?

Learn a comprehensive overview to prepare sponsors and sites for an FDA inspection.

Watch Now

Webinar

Unlocking Global Potential: Partnering Across Varying Sites in Study Startup

Join us as Advarra experts outline how sponsor organizations can work with various site types across trials and adapt their resources accordingly.

Watch Now

Webinar

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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Stuart Cotter

Latest Posts by Stuart

Re-air: Not if, but When: A Study Manager’s Guide to Adaptability and Incoming Trends

Not if, but When: A Study Manager’s Guide to Adaptability and Incoming Trends

Checklist to Reduce Burden on Sites and Patients

Sponsors: Are Your Sites Ready for an FDA Inspection?

Unlocking Global Potential: Partnering Across Varying Sites in Study Startup

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

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

Best Practices in Pre-Screening Includes Use of Technology

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

How to Be Research Ready: Today and Beyond

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

4 Reasons Your Institution Needs an eRegulatory System

Ready to Advance Your Clinical Research Capabilities?

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