Support specific to clinical research
- Clinical Trials Office
- School of Medicine Clinical Research Unit
- Institutional Review Boards (IRBs)
- Investigational Drug Service
- Managing a clinical research project (link to NHLBI web site)
- Compliance and training (radiation, chemical, biosafety, conflict of interest, misconduct, etc.)
- Material Transfer Agreements
- Intellectual property and entrepreneurial activities
Current NIH page limitations for grant proposals
“Boilerplate” documents and information for inclusion in grant proposals
- SOM core facilities
- Core facilities handbook 2013
- Moving your lab within UVA (Environmental Health & Safety checklist for decommissioning labs
- NEW 2/14 – Acknowledging the use of core equipment in your publications
- Center for Comparative Medicine (description)
- Sample data-sharing plans (NIH site)
- Tool for the development of NSF data management plans (from the University of California)
- Intellectual property management plans site (NIH site)
- Model organism sharing plans (NIH site)
- NIH Genomic Data Sharing Policy (and guidance for developing GWAS data-sharing plans)
- UVA institutional information for proposals
- Federal rate agreement (F&A and fringe benefits rates)
- Proposal preparation and submission checklist
- Help with grants.gov electronic submissions
- Internal pre-review of grant proposals: a best-practices document
- Descriptions of NIH study sections (NIH Center for Scientific Review)
- The NIH application cover letter
- NIH “All About Grants Podcast”
- Help with other NIH-required sections (animals, research subjects, resource sharing plans, etc.)
Clinical research-specific topics
- Assistance with developing clinical study budgets (Clinical Trials Office)
- Developing NIH clinical research proposals (NHLBI site)
- Navigating UVA regulatory compliance requirements