Electronic Clinical Research Information System (eCRIS)

eCRIS, OHSU's electronic Clinical Research Information System, is an institution-wide computer application for the budgeting, financial management, contracting, and study management, including subject tracking and regulatory reporting and document management, of OHSU clinical research studies. The system increases the efficiency, effectiveness, accuracy, and compliance of clinical research at OHSU. Studies involving prospectively consented human subjects are required to track their subjects in eCRIS though other types of studies are welcome to use the system. Read more about which studies need to use eCRIS.

eCRIS Leadership


eCRIS AdoptionSchedule Date
Phase 1 Go Live: Campus Wide Optional Use 22-Jul-13
Phase 2 Go Live: Invoicing/Payment Reconciliation Available 13-Nov-13
All new studies submitted to IRB require eCRIS/Knight Go Live 29-Jan-14
Phase 3 Go Live: Additional Functionality (see release schedule below)
Summer 2014
All existing studies migrated to eCRIS 14-Jul-14


Phase 3 release schedule

eCRIS data will be available by mid-June for reporting purposes in the Sponsored Project Data Repository (SPDR). Reports have been requested and will be made available as they are built. If you would like a report built containing eCRIS data, please consult the current eCRIS report list on the eCRIS Bridge Site to see if it has already been requested. If the report has not already been requested, please send the request including a mock-up of the report to eCRISsupport@ohsu.edu and its development will be prioritized and scheduled.

eCRIS Access and Training

The Clinical Research Billing Office (CRBO) provides training and education for eCRIS. The following steps are required to access eCRIS:

Optional one-on-one training is available after taking the overview class. Email to schedule. See the eCRIS Training and Education page for more information on requirements and signing up for training.

eCRIS Support

eCRIS support is available by emailing The mailbox is continuously monitored between the hours of 8:00 a.m. and 4:00 p.m. Monday through Friday. Inquiries are processed in the order in which they are received unless marked high importance. High importance inquiries are those which prevent an end from proceeding through an eCRIS workflow or smartform and are given priority.


Ongoing Studies

As of November 13, 2013, eCRIS can be used to manage ongoing studies. For more information on how to enter ongoing studies, please refer to the ongoing studies section of the eCRIS User Manual. Existing subjects on ongoing studies can be bulk uploaded into eCRIS for you by ITG.  Refer to the Ongoing Study Subject Bulk Upload Instructions for information on how to do this. The template for transmitting the data to ITG is here.



eCRIS User Group - April 28, 2014, 3pm, CHH 3rd floor, room 3171 A/B

eCRIS Coffee Talk, Ongoing Studies - May 5, 2014, 1pm, UHS8B60


eCRIS Brownbag Presentations

May 6, 2013 -- Coffee Talk PowerPoint

November 14, 2013 - Coffee Talk Powerpoint


eCRIS User Environment Site

A user test environment is available to familiarize yourself with eCRIS outside of the production environment. Generic logins for all of the roles in eCRIS are available and listed on the login page.