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Resource Library

Frank Conte

Vice President, Strategic Partnerships, Advarra

Frank Conte has more than 20 years of experience in project management, research administration, and regulatory compliance. Conte’s background includes consulting with universities and hospitals, where he gained significant regulatory, compliance, and operational experience within the human subjects protections space and has led projects related to organizational and operational redesign, IRB and HRPP compliance, accreditation, and other related work. Conte also has noteworthy experience in the research administration technology space, helping organizations select, understand, implement, and effectively use software solutions.

Latest Posts by Frank

Blog

Budgeting for IRB Review: A Guide for HRPP Leadership

Internal IRB reviews are NOT free, contrary to popular belief. In this blog we outline practical steps for assessing and establishing IRB review cost

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5 min. read

Blog

Impact of sIRB Mandates on Study Teams

May 16, 2024

Much has been written about the impact of single institutional review board (sIRB) mandates on local IRBs and human research...

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6 min. read

Webinar

Navigating sIRB Complexities: An Interactive Session

Join us as we share insights, strategic priorities, and guidance for preparing your institution for sIRB mandates.

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Blog

What is an sIRB and Why Does my Study Need One?

Federal requirements have shifted to require most multisite clinical trials to rely on a single IRB (sIRB) for trial oversight.

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6 min. read

Webinar

sIRB 101: An Introduction to Relying on an External IRB

Learn the basics of working with an sIRB and gain insights for successful sIRB relationships with external IRB partners.

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Blog

How Single IRB Review Mandates Help Research Sponsors

The proposed single IRB mandates will impact FDA-regulated research, potentially altering existing practices at organizations.

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4 min. read

Blog

Beginner’s Guide to Single IRB Mandates

More governing bodies are starting to opt for single institutional review board (sIRB) review as a way to streamline research operations.

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5 min. read

Webinar

Budgeting for Single IRB Review

A practical discussion of budgeting considerations for sIRB review, including strategies for policies around external IRB reliance.

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Blog

A Checklist for Optimizing Clinical Trial Study Startup Activities

This checklist outlines key milestones and considerations for sites and sponsors in the clinical trial study startup process.

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7 min. read

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Frank Conte

Latest Posts by Frank

Budgeting for IRB Review: A Guide for HRPP Leadership

Impact of sIRB Mandates on Study Teams

Navigating sIRB Complexities: An Interactive Session

What is an sIRB and Why Does my Study Need One?

sIRB 101: An Introduction to Relying on an External IRB

How Single IRB Review Mandates Help Research Sponsors

Beginner’s Guide to Single IRB Mandates

Budgeting for Single IRB Review

A Checklist for Optimizing Clinical Trial Study Startup Activities

Dive Deeper into Study Startup Optimization

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