On-Demand Webinar

Budgeting for Single IRB Review

Single IRB (sIRB) review has become a standard requirement for many types of research: NIH, OHRP, and others now mandate this centralized oversight for most multisite studies.

But not all researchers are fully aware of these requirements, which can lead to operational and financial challenges, particularly for grant-funded projects. Additionally, some institutions have more robust processes to support such mandates than others.

Join this webinar for a practical discussion of budgeting considerations for sIRB review. Experts in institutional research and human subject protections will review strategies for developing policies around external IRB reliance and approaches to accurately budgeting and planning for sIRB review, including case study examples from the University of Rochester.

Learning Objectives:

After attending this free webinar, attendees will be able to:

  • Describe what researchers and HRPP professionals should know about budgeting and planning for sIRB oversight
  • Identify the sIRB options that are available for researchers
  • Recognize ways institutions and IRB administrators can support sIRB requirements

Presented By

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Frank Conte

MS

Vice President, Institutional Partnerships
Advarra

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Kelley O’Donoghue

MPH, CIP

Associate Vice President for Human Subject Protection
University of Rochester

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Who should watch?

IRB members, administrators, and other human subject professionals supporting grant-funded multisite research projects. Grants administrators involved in supporting the research grant application process. Principal investigators and other research professionals developing and conducting research involving multiple investigators and site locations

CE Credits

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.

This event may qualify for continuing education (CE) credits. Please check with your professional organization(s) to determine whether the event meets their CE eligibility requirements.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour

Register Now