Clinical Translational Research (CTR) Portal
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CTSI's Clinical Translational Research (CTR) Portal is an interactive, web-based system designed to provide targeted and secure access to research project information. The system is available to research teams at the University of Minnesota and in our communities.
Continue reading to learn more about the CTR Portal, find answers to Frequently Asked Questions, and download forms and user guides.
CTR Portal overview: Frequently asked questions
The Clinical Translational Research (CTR) Portal is an interactive, web-based system designed to provide targeted and secure access to research project information. Among CTSI’s primary goals is the creation of an academic home and an adaptable, sustainable infrastructure for clinical translational science research at the U of MN. One way we are meeting this goal is by creating the Portal to provide targeted and secure access to research project information. Our goal is for the Portal, while first designed to meet CTSI’s core business needs, to become an efficient mechanism for accessing and sharing accurate, timely information among the clinical research community. The CTR Portal is intended for use by the entire research team - investigators, coordinators, project managers, finance staff, and administrators.
Initial functionality of the Portal is designed to help CTSI manage the business of the institute: intake of new projects; tracking services provided to research teams; and invoicing for those services. Also, with the recent receipt of the CTSA grant, the new Request for Services system helps CTSI collect information about projects required for reporting to the NIH.
Additional functionality will be developed in the coming months and years. The development team is actively engaged in aligning all CTSI systems with existing and planned enterprise systems.
As of August 1, 2011, the CTR Portal provides a single, secure point of access to:
- News and information about CTSI and the Portal
- Links to helpful tools and systems, such as the clinical research unit scheduling system and UMN Profiles
- Access to create a new project and request CTSI services
- Access to view and approve invoices for CTSI services
- A list of your projects included in the CTSI database
Anyone with a University of Minnesota x.500 (internet ID and password) may log in to the CTR Portal. The information you can access once you log in depends on your role and individual system rights. Access to project information is provided by the Principal Investigator (PI). Download the CTR Portal Access Request Form.
If you do not have a University of Minnesota x.500 (internet ID and password). First, go to: https://ctsi.ahc.umn.edu/portal/. If you already have a UMN Guest Account, click "Log In" and you will be directed to the Portal home screen..
If you need to create a UMN Guest account, click "Setup Guest Account," and enter the information requested by the form. You will receive a confirmation email and gain access to the Portal immediately.
If you update your x.500 (Internet ID), e-mail CTSI at firstname.lastname@example.org in order for us to update your CTR Portal login information. Once we’ve updated your login information to reflect your new x.500 ID, you will be able to successfully login to the Portal with your new x.500 in order to access your existing project information.
The CTSI CTR Portal is designed to work with most web browsers for PCs and Macs. We recommend you always use the most current version of your web browser to make sure our web pages display correctly, and that you have the latest security updates.
We recommend the following supported browsers:
When using the Portal, please use one of the recommended supported browsers listed above. We do not recommend using any unlisted or older versions of browsers because you may experience compatibility issues.
CTR Portal features and tools: Frequently asked questions
What is the definition of a "project" at CTSI?
A project is an individual research protocol or study. A project may have multiple funding sources or sponsors, and a single funding source or sponsor may fund multiple projects.
What does the "status" of my CTSI project mean?
- Registered: A project that is registered within the CTR Portal, but isn't currently receiving CTSI services. This includes projects that were registered only, and projects that had requested CTSI services (and the request was possibly accepted) but are no longer pursuing CTSI services.
- Active: A project that is in process and is currently or was receiving services from CTSI.
- Project Complete: A project that has met all criteria to be considered finalized and complete.
- Pre-CTSI: A project that was brought over from the General Clinical Research Center (GCRC) that has been completed, halted, or has not requested CTSI services.
What information is included in a project record?
- CTSI ID or project number, titles, and abstract or project description
- CTSI Status
- Sponsored account information
- Budgeted hours for CTSI services
- Other codes and identifiers: Electronic Grants Management System (EGMS); National Institutes of Health (NIH); ClinicalTrials.gov; Time and Study Collection System (TASCS); Institutional Review Board (IRB)
- Personnel assigned to the project
- CTSI service lines used by the project
Why can’t I see a project?
It may be because you are not actively assigned to the project or because the project has not yet been registered within the CTR Portal. If you are not yet assigned to the project, see instructions below.
The title of my study has changed. How do I update that?
If your study is approved by the University of Minnesota IRB, complete the IRB Add/Change/Remove IRB Study Titles form and forward to email@example.com. If the study is IRB-exempt, complete the CTSI Project Update Request Form and forward to firstname.lastname@example.org.
I need to add a staff member to my project. How does a member of my research team gain access to my study in the Portal?
Is your study approved by the University of Minnesota IRB?
- If yes, forward a copy of the IRB Add/Change/Remove IRB Study Personnel form and the IRB approval letter to email@example.com.
- If no, complete the CTSI Access Request Form and forward to firstname.lastname@example.org.
The members of my project team have changed; how do I add the new staff to the project in the Portal?
Anyone with active access to a project can request to add individuals to or remove individuals from the project, thereby either adding or restricting access to project information. To modify access to your project, complete the CTR Portal Access Request Form and return the form to email@example.com or 612-625-2695 (fax). Note, if you are requesting access to the CTSI Scheduling System, the Principal Investigator must initial and sign the form.
My accountant or department administrator needs access to my project information. How do I make that happen?
How do I request services from CTSI?
Log in to the CTR Portal. Click on the "New Request" button to start a request for a new or existing project.
Several of the questions CTSI asks are the same as those on the University of Minnesota IRB application. Why do I need to answer the same questions twice?
As a recipient of a Clinical and Translational Science Award, CTSI is required to report detailed information about our institution’s research activities in an annual progress report to the National Institutes of Health (NIH).
CTSI is also working closely with sponsors of University-wide enterprise systems, such as the Solutions for Integrated Research Compliance initiative, to encourage seamless data sharing among research-related systems.
What if I only want specific services such as biostatistics assistance, clinical procedures, or access to research facilities?
Requests for limited assistance, such as biostatistics or access to space, are processed in a timely manner. Please follow the instructions above to request services.
When can a study begin using services?
The PI will receive a correspondence from CTSI within ten business days of submission. This correspondence will provide detailed information about next steps and the process for accessing services. This time frame will vary depending on the service requested. For example, clinical research facilities and support staff are available after IRB approval is received and a CTSI in-service workshop is completed.
How long does a request for services review take to complete?
No more than ten business days.
What does the status of my request mean?
- Pending Submission: A request has been saved, but not yet submitted. You may modify the request, or submit it to CTSI for review.
- In Review: A request is currently being reviewed by CTSI; you may view your request, make modifications to the content, or submit additional service requests.
- Completed: A request that has been reviewed by CTSI. No further modification can be made.
I need to change or update a request for services. How can I do this?
If your request status is classified as “Pending Submission” or “In Review”, you may access your request and make changes, save your progress, or submit additional service requests. If your request status is marked “Completed”, please contact the CTSI Research Navigator at 612-625-CTSI (2874) or firstname.lastname@example.org.
Who can I contact for help with my service request?
Contact the CTSI Research Navigator at 612-625-CTSI (2874) or email@example.com.
The Invoice Manager module is used by CTSI and departmental personnel to distribute, review, and approve charges for services provided by CTSI.
How can I review and approve invoices?
Why can’t I see or review an invoice?
It may be because you are not actively assigned to the project or because the project hasn't yet been registered within the Clinical Translational Research Portal. For assistance please send a message to CTSI at firstname.lastname@example.org.
I need to change the EFS chart string for my study. How do I request the change?
Members of the research team with invoice approval rights can update chart strings for the study. For assistance please send a message to email@example.com.
What is the purpose of the Scheduling System?
The Scheduling System facilitates scheduling of research participant visits for studies at the Delaware, Masonic, and Lillehei Clinical Research Units. All visits at these facilities must be scheduled through this web-based system.
When is my study added to the Scheduling System? When can I begin scheduling participant visits in a CTSI facility?
A study is added to the Scheduling System after IRB approval is received AND either: 1) an in- service workshop is held to train CTSI clinical staff members in the conduct of the protocol; or 2) the Clinical Research Implementation Services (CRIS) Manager determines that an in-service is unnecessary. The PI will receive email correspondence regarding this decision.
I have a staff member that needs access to the CTSI Scheduling System. How does that happen?
I need technical assistance with the Scheduling System. Who can help me?
Contact Trung Ngo at 612-626-5203 or firstname.lastname@example.org.
The Toolkit provides links to CTSI or University of Minnesota systems and information related to clinical and translational science research, including:
- Time and Study Collection System (TASCS)
- University of Minnesota Institutional Review Board
- UMN Profiles
- CTSI Scheduling System
CTR Portal forms and user guides
Visit the Forms and Templates page to download the Access Request Form, Project Update Request Form, and the Invoice Approver User Guide.