Summer 2026 IRB Newsletter

July 28, 2026

 

IN THIS IRB NEWSLETTER:

Understanding the Policy on Privacy in Research: An interview with Alexis Goltra

Request for Feedback: Drop-In hours and IRB 101/IRB Topics

Husky Tip: Need NHSR Documentation for a Publication?

Make Sure your Submission is Review-Ready

Upcoming Events and Training

Understanding the Policy on Privacy in Research: An interview with Alexis Goltra

We recently interviewed Alexis Goltra about Northeastern’s Policy on Privacy in Research (Policy 127) which was published in January 2026. As NU’s Chief Privacy Officer and Senior Privacy Attorney, Alexis Goltra is responsible for overseeing the university’s global privacy and data protection compliance program. In the interview, Alexis shares his expertise and draws on that experience to break down how Policy 127 helps researchers comply with global privacy laws and data protection requirements while offering practical guidance that is straightforward to implement in the research setting.

Find the whole interview here.

Request for Feedback: Drop-In hours and IRB 101/IRB Topics

We’d love to hear from you about our educational offerings, so we put together a short 4-question survey to gather your feedback.

Over the past year, we’ve hosted 185 drop-in hours and met with 400+ researchers during those sessions. As we continue to expand and improve these offerings, we’d love your feedback. Your input will help us better understand what topics, formats, and resources you would find most valuable during our Drop-In Hours and IRB 101/IRB Topics sessions moving forward.

Find our short feedback survey here.

As always, please be sure to visit our Calendar of Events for the most up-to-date educational offerings, including drop-in hours, as well as details on how to join each session. Please note that we will be switching from Zoom to Teams effective August 10th. The Teams link will be on the calendar.

Zoom Changes

We understand that changes to Zoom may affect how some research teams conduct their studies. If your study procedures will change as a result of moving to a different platform, please note the following:

  • Expedited and Full Board studies: If you are changing from Zoom to another platform, you must submit a modification to the IRB before implementing the change.
  • Exempt studies: A modification is not required if you are changing from Zoom to Northeastern Microsoft Teams, provided no other study procedures are changing.

For any questions about the change beyond how to modify your IRB study, please submit an IT service ticket. If you have questions about the Zoom transition that are not related to how to submit a modification to your IRB study, please submit an IT Service Desk ticket.

Husky Tip: Need NHSR Documentation for a Publication?

Occasionally, a journal may request documentation that an activity was determined Not Human Subjects Research (NHSR) at the time the work was conducted. This can be challenging if you self-determined that the activity did not require IRB oversight. If you find yourself in this situation, we recommend completing Human Subjects Research Determination Form. As you work through the form, it should become evident whether your project does or does not meet the regulatory definition of human subjects research.

This is a self-determination form and does not need to be submitted to our office, In our experience, most journals accept a completed Human Subjects Research Determination Form as sufficient documentation if the activity did not require IRB oversight . Because the work was already conducted, the DHR/IRB cannot perform a retroactive IRB review or issue a retroactive determination.

Make Sure your Submission is Review-Ready

Our practice is to conduct an administrative pre-review of all submissions before they are assigned for IRB review. Submissions that are not review-ready will be returned to the research team before the IRB review begins. This helps ensure reviewers receive complete, consistent applications and allows them to focus on the substantive ethical and regulatory aspects of the proposed research.

How can you prepare a review-ready submission?

Before submitting, please consider whether:
• Your entire submission and all study documents are complete and consistent.
• Every section of the protocol fully addresses the questions being asked. .
• The study procedures are described clearly enough for a reviewer to understand how the research will be conducted.
• All participant-facing materials accurately describe the study procedures.
• All study documents, including participant-facing material, recruitment materials, data collection instruments, and applicable forms are included with your submission and signed, as required.

You can also use AI tools to help identify missing materials or sections that are incomplete. See Leveraging AI for Easier IRB Submissions.

Questions?
Attend  Drop-In Hours or contact our office.

Upcoming Events and Training

Our Summer schedule of IRB 101 and IRB Topics is now available, Summer is typically a lighter season for educational programming, but we look forward to expanding our offerings during the fall semester.. As always, please be sure to visit our Calendar of Events for the most up-to-date educational offerings, including drop-in hours, as well as details on how to join each session.

Suggestions or feedback? Complete our DHR Satisfaction Survey or email [email protected]!

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