Welcome to the Office of Research Compliance
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Office Information

Office: Delany Hall Room 305
Hours: Mon – Fri, 9 am – 5 pm

Please call or email ahead to schedule an appointment.

 

IAbout the Office

The Office of Research Compliance administers and facilitates regulatory compliance and assurance efforts associated with research activities at CUNY Queens College. Navigate the Office of Research Compliance dropdown menus at the top of this page to find information, policies, and guidance related to Human Subjects Research (HRPP and IRB), Research Involving Animals (IACUC), Conflict of Interest, Export Control, Institutional Biosfatey, Responsible Conduct of Research, and Research Agreements.

IIRB News

IRB Submissions and Review will be moving to a new system, Cayuse, beginning on August 3, 2026. Many investigators may already be familiar with Cayuse, which has been operational for Grant Submissions since it went live  in FALL 2025. Here is a letter fron Lynda Mules, CUNT’s Executive Director of Research Compliane, that explains the process and the timeline.

 

 

Dear Colleagues,

As we continue with the implementation of Cayuse Human Ethics as our new IRB submission and review platform, we want to remind you of upcoming dates.

Key Timeline (Upcoming Milestones)

June 26

Last day to submit an Initial Application, Amendment, or Event Report in IRBManager (NOTE: Your campus may have an earlier date based on workload or other criteria.)

July 6

Start of IRB “Quiet Period”

  • HRPP staff work to migrate legacy data from IRBManager to Cayuse Human Ethics
  • Most submission and review activities are temporarily paused to support system transition and data preparation
  • Training materials and resources are finalized

August 3

Cayuse Human Ethics official “Go Live”

What to Expect in July

Starting July 6, we will temporarily pause new submissions to the IRB. This includes new applications, amendments to approved projects, and other submission types.  The purpose of the quiet period is to accommodate the transfer of data from IRBManager to Cayuse Human Ethics. 

If you have an urgent need (because of federal funding, for example) to submit a new IRB application, amendment, event (such as non-compliance or an adverse event) or other submission, please contact your HRPP Coordinator for guidance.  

What to Expect in August

  • Active researchers, IRB members, and HRPP staff will be able to log in to Cayuse using CUNY Login and access the Human Ethics module.
  • New users will be able to request access to Cayuse (details to come).
  • Resources such as videos, SOPs, and guidance documents will be shared.
  • Live training sessions will be scheduled.

Coming Soon

  • More details about legacy data migration and how researchers will be able to access information and materials for active migrated projects.
  • Access to a recorded demo of Cayuse Human Ethics.
  • Information about training and access to resources.
  • Instructions for accessing Cayuse Human Ethics.

Questions

Answers to frequently asked questions are available on the CUNY Office of Research website, and more information will follow. If you have other questions or need assistance, please contact your campus HRPP Coordinator. You can also reach the RIC Cayuse team at CUNY_eRA@cuny.edu.

Moving to Cayuse Human Ethics will bring human subjects research into CUNY’s enterprise electronic research administration system. Thank you for your cooperation and continued commitment to ethical and impactful research at CUNY as we move toward a more integrated and efficient infrastructure.

Sincerely,

Lynda Mules, MLA, CIP
University Executive Director of Research Integrity and Compliance
Office of Research
The City University of New York
Learn more about Cayuse: www.cuny.edu/research/electronic-research-administration/

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General Information about the IRB

See the CUNY Researcher Handbook for information, policies, and guidance related to conducting research. See Chapter 5 of the CUNY Researcher Handbook and the CUNY Research Compliance site for information, policies, procedures, and guidance specifically related to research compliance.

 

Human Research Protection Program at Queens College

The CUNY Human Research Protection Program (HRPP) is responsible for the protection of the rights and welfare of human subjects in research projects conducted at CUNY or by CUNY faculty, staff and students and Research Foundation CUNY staff. All research activities involving human subjects must be reviewed and approved by the CUNY HRPP or CUNY University Integrated-Institutional Review Board (CUNY UI-IRB) prior to implementation.  The information below will provide Queens College researchers with the information needed to access CUNY policies and procedures, as well as the tools to submit a complete IRB application. All CUNY’s institutional policies concerning HRPP issues are located at https://www.cuny.edu/research/research-compliance/human-research-protection-program/hrpp-policies-procedures/.

 

Toward the end of the above page, you will find template for consent forms, assent forms and other materials that may be of use as you develop your IRB application.

How to Apply

All submissions to the HRPP/IRB must be made through IRBManager using your CUNYfirst credentials

There is also a detailed instruction manual that can be found inside the IRBManager system once you log in to your profile.

Is IRB review required for my project?

If you are unsure whether your project requires CUNY UI-IRB or HRPP review, please read the document When is CUNY HRPP or IRB Review Required? For further assistance in determining whether an activity constitutes human subjects research requiring review by the HRPP/IRB,  contact Paul Kran, Director

 

Guidance and Development of the IRB Application

  • The complete list of CUNY HRPP Policies, Procedures Guidelines can be found in the CUNY HRPP website. Review the policy documents while designing your IRB protocol.
  • A list of Informed Consent templates are available in the Informed Consent section of the CUNY HRPP website. Please use these templates when developing your informed consent process and creating consent documents.
  • A note about the annual check in: The main thing we look for when reviewing the Annual Check in to ensure all active staff are up to date on their trainings.  Therefore, we advise removing inactive staff and adding additional staff be done via an amendment to the protocol prior to submitting the annual report form.

 

CITI Training

First time CITI users should access the CITI website at www.citiprogram.org. For further information about the CUNY HRPP CITI Training in the Protection of Human Subjects, please see the CUNY policy: CITI Training in the Protection of Human Subjects.

All CUNY faculty members, postdoctoral scholars, graduate and undergraduate students involved in animal research must complete the Collaborative Institutional Training Initiative’s (CITI) on-line training prior to IRB IACUC approval of a new or an amendment application that requests the addition of personnel.All CUNY faculty members, postdoctoral scholars, graduate and undergraduate students involved in animal research must complete the Collaborative Institutional Training Initiative’s (CITI) on-line training prior to IRB IACUC approval of a new or an amendment application that requests the addition of personnel.

Please note that ALL researchers are required to complete Responsible Conduct of Research.

As of June 2025.  CUNY has enabled SSO login to the CITI program and all its courses.  Use your CUNYFirst login to access.  Full Instructions are at the link below.

https://www.cuny.edu/research/research-compliance/training-education/citi-training/.

Many of you may have experienced difficulties in terms of getting your training date to appear on the protocol even when the training is up to date. Logging into the CITI system via SSO one time should correct this issue.  You may log right off without doing any additional training and that should correct the issue.

Human Subjects Protection Basic Course

All CUNY faculty members, postdoctoral scholars, graduate and undergraduate students involved in human subjects research as key personnel must complete the Basic Course in the protection of human subjects prior to Institutional Review Board (IRB) approval of their protocol. Certificate of completion of the basic course is valid for three years.

Human Subjects Research Refresher Course

Key personnel of human subjects’ research protocols must complete a refresher course every three years.​

Researchers from outside Queens College who would like to recruit participants or collect/review data from the campus do not require IRB approval IF no QC researcher is involved in study design or data analysis.  Such requests are handled by a committee within QC’s Office of Institutional effectiveness.  Follow the link for guidance.

 

Staff:

Paul Kran

Director for Research Compliance
HRPP/IRB Administrator, College Conflicts Officer, Export Control Officer, Research Agreements Point of Contact
Phone: 718-997-5415
Fax: 718-997-5549
Paul.Kran@qc.cuny.edu

Sandra Yauri
Research Compliance Manager-IACUC
Phone: 718-997-5160
Fax: 718-997-5549​
Sandra.Yauri@qc.cuny.edu

Kate Pechenkina
College Research Integrity Officer

Contact Kate for actual or suspected instances of  plagiarism, data fabrication or falsification and matters concerning potential violations of any CUNY policy on research.  More general inquiries should be addressed to the director.

718-997-5210

Kate.Pechenkina@qc.cuny.edu

 

IACUC Deadlines, Spring 2026

Submission Deadline Dates

Wednesday, January 14

Wednesday, February 11

Wednesday, March 11

Wednesday, April 15

Wednesday, May 13

Review Meeting Dates

Wednesday, January 28

Wednesday, February 25

Wednesday, April 1

Wednesday, April 29

Wednesday, May 27

   Overview

Implementation of New Common Rule

More on CITI Training

IRB Submission and Meeting Dates, Summer/Fall 2025

Submission Date Meeting Date
1/16/2026 2/6/2026
1/29/2026 2/19/2026
2/13/2026 3/6/2026
2/26/2026 3/19/2026
3/27/2026 4/17/2026
4/9/2026 4/30/2026

          4/24/2026

          5/15/2026

          5/7/2026

          5/28/2026

        5/22/2026

          6/12/2026

          6/4/2026

          6/25/2026