Onboarding Summer Student Researchers: Guidance for Summer 2026
The LSUHSC-NO IRB is gearing up for Summer Research 2026. If you plan to involve summer students in human subjects research, now is the time to prepare. To help ensure timely approval and a smooth onboarding process, please review the important deadlines, requirements, and submission tips below.
If you plan to add a summer student to an existing IACUC or IBC protocol, please contact the appropriate office for guidance on required trainings and amendment instructions. These resources are also available on our committee webpages.
IACUC Office: IACUCoffice@lsuhsc.edu
IBC Office: IBCoffice@lsuhsc.edu
Students participating in the following programs should submit to the LSUHSC-NO IRB if their projects involve human subjects research:
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LSUHSC Summer Research Internship Program for Medical Students (LSUHSC-NO)
Directors: Tsien, Sherman, Zabaleta -
LSUHSC Summer Research Internship Program for Medical Students (LSUHSC-Baton Rouge)
Directors: Tsien, Sherman, Zabaleta, Reed -
The Robert A. Winn Clinical Investigator Pathway Program (Winn CIPP)
Directors: Miele, Tsien -
LSUHSC NIH-T35 Alcohol Research Program for Medical Students
Directors: Edwards, Molina -
Research Elective Medical Students – MCLIN198
Director: Tsien
To allow sufficient time for review and approval:
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Submit your Kuali application by April 15, 2026
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Target IRB approval by June 1, 2026
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This timeline applies to:
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New protocols
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Amendments adding students to existing approved protocols
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Submissions after April 15, 2026 may not receive approval by June 1, which could delay student participation.
To avoid delays during review:
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Complete all required trainings and COI disclosures before submitting.
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Use LSUHSC-NO IRB templates and remove instructional text before uploading.
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Upload all documents as PDFs.
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Submit clean documents (no tracked changes unless responding to revisions or submitting an amendment).
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Clearly and concisely describe your research activities.
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Specify the number of participants or records you expect to enroll and justify that number.
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List all data elements or variables you plan to collect and upload related tools (REDCap forms, surveys, etc.).
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Explain how you will access the data sources.
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Indicate whether PII or PHI will be collected and describe how it will be stored and protected.
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Provide certified translations for any non-English participant-facing materials.
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External researchers: Review IRB website guidance before submitting.
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Single IRB reliance studies: Consult IRB website guidance for requirements.
LSUHSC-NO, under the purview of the Office of Compliance Programs and the Office of Research Services, requires specific training for individuals involved in research. The Office of Research is responsible for confirming compliance with the training and disclosure requirements for all HSC investigators including those listed in the initial application and those added after study approval through an amendment request.
Training Providers
| Providers | Access |
| CATS | CATS is a web-based training program managed by the Office of Compliance Programs (OCP). For more information about institutional training requirements and to access CATS, please visit the OCP website. All training requests should be sent to the Office of Compliance Programs nocompliance@lsuhsc.edu. |
| CITI | Important for LSU Health-NO Investigators: Once your account is created, log in to CITI using your LSU Health-NO credentials through Single Sign-On (SSO), following the steps in this document. Logging in through SSO ensures your CITI training records automatically sync with Kuali. |
| Kuali | Annual COI disclosures are submitted through the Kuali Research COI module. Information about COI disclosure and access to the Kuali Research COI module is found here. |
Any employee, faculty, staff or student of LSUHSC-NO considered to be a key personnel in human subjects research (HSR) OR engaged in the conduct of HSR is required to complete HRPP- and institution-mandated research training prior to the initiation of research. IRB approval of a research study will not be issued until all training requirements are met. Individuals who are not key personnel AND not engaged in HSR, are exempt from training requirements described below
Key Personnel: any individual responsible for the design, conduct, or publication/presentation of research results.
Engaged: an individual who intervenes or interacts with living individuals for research purposes, or obtains individually identifiable private information for research purposes.
Training requirements for external investigators - non-LSUHSC personnel engaged in a LSUHSC-associated study - are described here.
Training Course |
Frequency |
Training Provider |
Required for Personnel Involved in |
|
Biomedical Research Basic - |
Every 3 years |
Biomedical research |
|
|
Social & Behavioral Research Basic -Initial & Refresher |
Every 3 years |
Social and Behavioral research |
|
|
Good Clinical Practice - |
Every 3 Years | CITI | NIH-funded clinical trials or FDA-regulated drug or device studies |
|
Conflict of Interest in Research Disclosure |
Annual | Kuali Research | All HSR studies |
|
Conflict of Interest in Research Training |
Every 4 years | CATS | All HSR studies |
|
HIPAA Privacy-- Research |
Annual | CATS | All HSR studies |
|
Bloodborne Pathogen |
Annual (high risk) or every 5 years (low risk) |
CATS | All HSR studies |
|
Shipping Biological Materials |
Every 2 years | CATS | Individuals shipping biospecimens in any HSR study |
Contact the IRB by email for questions & problems: IRBoffice@lsuhsc.edu