Data Safety and Monitoring of Clinical Trials
In accordance with the NIH’s policy on data and safety monitoring of clinical trials NIH Grants Policy Statement (Part II, Chapter 4), the grantee must submit a data and safety monitoring plan for review and approval.
Prior Approval of Delayed Onset Research Involving Human Subjects and Live Vertebrate Animal Subjects
Prior to the start of the K12 award period, all scholars that conduct research involving human subjects and/or live vertebrate animal research are required to obtain prior approval from the National Institutes of Health. The NCATS Prior Approval process requires that all regulatory approvals be in place before the study may begin and may take 30 days or more. For more information, visit the NCATS website.
Human Subject Projects Documentation Required:
- Completed the NCATS Prior Approval Human Subjects Form (form to be provided)
- IRB-approved research protocol (eProtocol application is not considered a research protocol)
- IRB-approved informed consent, verbal consent transcript, assent and parental permissions documents, or documentation of IRB waiver, if applicable
- Summary of request, line item budget and detailed budget justification for the specific aspects of the proposed study that will be supported by NCATS funds
- Summary of parent study, if applicable
- NIH Biosketches for K12 Scholar, Research Mentor, and each Key Personnel involved in the proposed study
- Institutional letter attesting to Human Subjects Protection Training (i.e., CITI Training Record – Group 7: IRB BioMed/GCP Research for All Medical Investigators and Staff) completed by the K12 Scholar, Research Mentor and study Key Personnel
Animal Projects Documentation Required:
- Completed NCATS Prior Approval Live Vertebrate Animals Form (form to be provided)
- Research/scientific protocol
- APLAC/IACUC approval letter
- NIH Biosketches for the K12 Scholar and Research Mentor