
Frank Conte
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 Conte

Budgeting for IRB Review: A Guide for HRPP Leadership
At institutional research programs around the U.S., there exists a pervasive myth: internal institutional review...
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Impact of sIRB Mandates on Study Teams
As sIRB mandates reshape the clinical trial landscape, study teams must navigate unique challenges while...
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Navigating sIRB Complexities: An Interactive Session
Got questions about sIRBs? Join experts as they share insights and priorities, plus a Q&A...
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What is an sIRB and Why Does my Study Need One?
Single IRB (sIRB) review streamlines oversight for multisite trials, reducing administrative burdens while ensuring participant...
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How Single IRB Review Mandates Help Research Sponsors
The Food and Drug Administration’s (FDA’s) proposed single institutional review board (sIRB) mandates are in...
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