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Frank Conte

Vice President, Institutional Partnerships, Advarra

Frank Conte has more than 20 years of experience in project management, research administration, and regulatory compliance experience. Conte’s background stems from consulting with universities and hospitals. Additionally, he has 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 significant experience in the research administration technology space, helping organizations select, understand, implement, and effectively use software solutions.

Frank Conte

Latest Posts by Frank

 
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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