Grant Pre-award Intake Form

This form contains logic, so please ensure all required fields are completed.

General Submission Information

New, Resubmission, or Supplemental?*

Is your submission new, a resubmission, or a supplemental?

This form may only be used for new, resubmission, and supplemental submissions. Please contact Pedspreaward@UCDenver.edu with your request. Please ignore the budget attachment below.

Please confirm the spelling.

Select
Caret IconCaret symbol
Does the Proposal Require a Mentor?*
Sponsor*

If possible, provide the eBRAP log number or identifies from a pre-application. eBRAP log numbers are two letters followed by six numbers. If you are a Partnering PI on a multiple-PI proposal, it will be followed by 'P' and another number.

(e.g. NIDDK)

Is CU a subaward from the sponsor listed above?*

(i.e. NIH, DOD, CDC, FDA, name of foundation, state)

Type of Submission*

The Federal Identifier may be found on the NIH summary of the previous submission. Enter N/A if your submission does not have a Federal Identifier.

(e.g. RFA-HL-22-011) Type in the funding opportunity announcement here or attach PDF in the drag-drop "attachments" box at the bottom of the form.

(e.g. foundation, association, state)

Identify the site/location/building where the majority (50% or more) of UCD's portion of the work will be performed.

Will subcontractors be included in this proposal?*

List each subcontractor and their administrator contact information.

Will there Be Children's Hospital Cost?*

Will the proposed project involve employees or other services at Children’s Hospital Colorado?

Research Protocols and Authorizations

Human Subjects Research (HSR)*

Does the proposed project involve human subjects research? If you are unsure if your study qualifies as human subjects research, review the definitions of human subjects research and clinical trials at https://grants.nih.gov/policy/humansubjects/research.htm

You do not need an approved protocol at the time of application. If the approval is pending, please answer "pending" and skip the date field.

Provide the most recent new approval or continuing review approval date (must be within the last year).

Classify the Research Focus*
Is this a Clinical Trial?*

If yes, a grant specialist will contact you to obtain additional information.

Predominate Type of Work Being Conducted*

Basic and Early Translational Research (also called fundamental or bench research): Research that provides the foundation of knowledge for the applied science that follows. This type of research encompasses scientific disciplines such as biochemistry, microbiology, physiology, cell biology, molecular biology, neuroscience, bioengineering, and pharmacology, and their interplay, and involves laboratory studies with cell cultures and animal model systems, as well as molecular/biochemical studies utilizing human specimens (including -omic studies) that address fundamental mechanisms of physiological function and disease. Additionally, this can include computational modeling, molecular epidemiology, and experimentation in other nonhuman model systems. Basic science also increasingly extends to behavioral and social sciences. Etiologic, Mechanistic and Clinical Efficacy Research: Research with human subjects that is focused on individual patients. Research conducted with human subjects (or on material of human origin such as tissues, DNA, specimens, and cognitive phenomena) for which an investigator (or colleague) directly interacts with human subjects or with individual subject’s data. Excluded from this definition are in vitro studies that utilize human tissues that cannot be linked to a living individual. Clinical Research includes: (a) mechanisms of human disease, including basic experimental studies in humans, (b), prevention and therapeutic interventions in controlled settings, (c) classical clinical trials, (d) development of new technologies evaluated at the individual human subject level and e) observational epidemiologic research. Health Services, Outcomes and Clinical Effectiveness Research: Research which studies the end results (outcomes) of the structure, processes and service delivery of the health care system on the health and well-being of patients and populations. This would include: a) epidemiological research modeling predictors of patient outcomes, b) pragmatic trials of preventive or therapeutic interventions in real world settings, c) studies of implementation and dissemination of evidence-based health care interventions, and d) epidemiologic surveillance studies

Purchase of Genomic Arrays Required?*

Also known as microarrays or bead arrays, genome arrays are a process to examine a piece of DNA on a glass slide to detect the different variants of sequence in the genome for the purpose of identifying/mapping variants.

Estimated dollar amount for the required genomic arrays.

Is Vertebrate Animal Research Involved?*

You do not need an approved protocol at the time of application. If the approval is pending, please answer "pending" and skip the date field.

Provide the most recent new approval or continuing review approval date (must be within the last year).

Are there Radioactive Materials?*

You do not need an approved authorization at the time of application. If the authorization is pending, please answer "pending" and skip the date field.

Are there Biohazards?*
Select
Caret IconCaret symbol

You do not need an approved authorization at the time of application. If the authorization is pending, please answer "pending" and skip the date field.

Are there Chemical or Mineral Hazardous Materials?*

Select all that apply.

Select
Caret IconCaret symbol

List authorizations for all chemical or mineral hazardous materials. You do not need an approved authorization at the time of application. If the authorization is pending, please answer "pending" and skip the date field.

Dual Use Research of Concern (DURC)?*

Is any agent or toxin in the proposed project classified as a DURC? For information, see http://www.phe.gov/s3/dualuse/Pages/default.aspx

For more information, see https://research.cuanschutz.edu/regulatory-compliance/home/export-control/export-control-home

Select
Caret IconCaret symbol

Budget

A detailed budget is required for the internal routing. Please provide general information about personnel and other costs. The Pre-award Grants Specialist will prepare a draft budget for your review.

How Will You Detail the Budget?*

Provide a list of (1) personnel, roles and their percent of effort each year (2) an estimate of other direct costs, such as supplies, animals, participant incentives, core facility services and Children’s Hospital costs (3) an estimate of any sub-recipient or consultant costs per year.

Attach Draft Budget, Budget Justification, Funding Opportunity Announcement, and any other pertinent files. PDF or Word document preferred.

Drag and drop files here or