Recent Announcements

Join us for one of our quarterly ClinicalTrials.gov training via Zoom.

Join us for one of our quarterly ClinicalTrials.gov training via Zoom. 

All training dates occur on a Thursday from 1:30pm – 3:00pm

Please look for an announcement from our office closer to the dates below:

        • August 4, 2022
        • November 3, 2022

The training will cover:

        • Overview of federal regulations, NIH policy, and journal requirements
        • How to properly register and maintain a ClinicalTrials.gov record
        • Results entry overview
        • Q&A 


ClinicalTrials.gov Training on Demand 

Unable to make the regularly scheduled ClinicalTrials.gov training?
Email us with your training or help request or view a video of a prior training here
 

We now offer consultation services!

We now offer consultation services!

The Human Research Compliance (HRC) Office is pleased to offer consultation hours to assist investigators, study coordinators, residents, and students with pre-review and other questions about IRB submissions.

Thirty minute appointments will be offered via Zoom during the following times:
  • Mondays: 11:00am - 1:00pm
  • Thursdays: 10:00am - 12:00pm, and 2:00pm - 4:00pm

Researchers may use the 30-minute time slot to receive assistance in:

  • Determining the feasibility of a project and possible regulatory implications
  • Pre-reviewing your draft IRB application, including your protocol and consent form
  • General questions about the IRB and other regulatory requirements

Submit a consultation request by cicking the button below, and we will be in touch with you within 1-2 business days.

Please note that these consultations are only advisory in nature; they do not take the place of a formal IRB review. If applicable, you will still need to submit your final application to the WCM IRB for formal review.

Not Receiving Our Newsletter?


The WCM IRB sends out all announcements and updates on the All Protocols and Research Coordinator Network (RCN) listservs. 

  • If you'd like to be added to the All Protocols listsserv, send an email to ALLPROTOCOLS-request@LISTSERV.MED.CORNELL.EDU. In the subject line, type "Subscribe AllProtocols [your first and last name and CWID]"
  • If you'd like to be added to the RCN listserv, send an email to RCN-request@MED.CORNELL.EDU.  In the subject line, type "Subscribe RCN [your first and last name and CWID]"




Newsletters & Announcements

IRB Newsletter June 2022

BRANYplus Extended Through Summer 2022

In response to the overwhelming positive feedback on the BRANYplus process and time to approval for new submissions, we are happy to announce the continuation of the program at least through the summer of 2022...

IRB Newsletter May 2022

The IRB website has been renovated and is now live!

We have recently created a more expanded website to provide our community with more information on the IRB as well as to provide helpful information to ...

IRB Newsletter March 2022

ClinicalTrials.gov Training

We are pleased to announce that our quarterly ClinicalTrials.gov training is now available to you whenever you want ...

IRB Newsletter April 2022

Do you know about our ClinicalTrials.gov training?

The Human Research Compliance team offers quarterly ClinicalTrials.gov trainings via Zoom! The next training is scheduled for:

Thursday, May 5th, 2022
1:30pm – 3:00pm
Registration Required to Attend
...

BRANYplus and WCM IRB Updates

Both available for the summer!

To the WCM Research Community, 

The WCM IRB began a partnership with the Biomedical Research Alliance of NY (BRANY) in December 2021 to implement BRANYplus, a temporary program to review initial submissions of proposed research studies. Due to...

IRB Consultation Services

The Human Research Compliance (HRC) Office is pleased to offer consultation hours to assist investigators, study coordinators, residents, and students with pre-review and other questions about IRB submissions.

Thirty minute appointments will be offered via Zoom during the following times...