Community-Engaged Cooperative Agreement - Rapid Response RFA
Project Title:
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Principal Investigator (name, rank, department):
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Number of Project Key Personnel
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Key Personnel 1 Name
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Key Personnel 1 Department
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Key Personnel 1 Rank
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Professor Associate Professor Assistant Professor Instructor Other
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Key Personnel 2 Name
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Key Personnel 2 Department
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Key Personnel 2 Rank
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Professor Associate Professor Assistant Professor Instructor Other
If 'Other', please specify.
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Key Personnel 3 Name
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Key Personnel 3 Department
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Key Personnel 3 Rank
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Professor Associate Professor Assistant Professor Instructor Other
If 'Other', please specify.
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Key Personnel 4 Name
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Key Personnel 4 Department
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Key Personnel 4 Rank
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Professor Associate Professor Assistant Professor Instructor Other
If 'Other', please specify.
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Key Personnel 5 Name
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Key Personnel 5 Department
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Key Personnel 5 Rank
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Professor Associate Professor Assistant Professor Instructor Other
If 'Other', please specify.
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Key Personnel 6 Name
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Key Personnel 6 Department
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Key Personnel 6 Rank
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Professor Associate Professor Assistant Professor Instructor Other
If 'Other', please specify.
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Key Personnel 7 Name
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Key Personnel 7 Department
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Key Personnel 7 Rank
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Professor Associate Professor Assistant Professor Instructor Other
If 'Other', please specify.
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Key Personnel 8 Name
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Key Personnel 8 Department
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Key Personnel 8 Rank
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Professor Associate Professor Assistant Professor Instructor Other
If 'Other', please specify.
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Key Personnel 9 Name
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Key Personnel 9 Department
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Key Personnel 9 Rank
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Professor Associate Professor Assistant Professor Instructor Other
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Abstract (30 lines max)
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Specific Aims (1 page max)
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Research Plan (6 pages max)
Specific Aims (1 page max)
Background and significance, translational importance, experimental design and methods, dissemination and implementation plan (4 pages max)
Study Milestones and anticipated outcomes with timeline (1 page max)
Contribution and summary of qualification of each contributing investigator (1 page max)
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References (no page limit)
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Does the proposed work involve human subjects?
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Yes No Unsure
IRB Approval
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Already have IRB approval for the proposed work Plan on submitting an amendment to an existing IRB approved project if funded Plan on initiating a new IRB application if funded IRB approval is not needed for the proposed work
IRB Number
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Please explain why IRB approval is not needed for project involving human subjects.
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Will this project be classified as a clinical trial?
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Yes No Unsure
Please provide more information on why you are 'unsure' about the proposed work being classified as a clinical trial.
Type of Clinical Trial
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Phase 0 drug clinical trial Phase I drug clinical trial Phase II drug clinical trial Phase III drug clinical trial Phase IV drug clinical trial Device clinical trial Non-FDA regulated clinical trial
Addressing Human Subjects (1 page max)
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Inclusion Plans for Women, Minorities, and Children (if not applicable, upload a document stating this)
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Data and Safety Monitoring Plan (DSMP) and Board (DSMB) (if not applicable, upload a document stating this)
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Does the proposed work involve live vertebrates?
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Yes No Unsure
IACUC Approval
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Already have IACUC approval for the proposed work Plan on submitting an amendment to an existing IACUC approved project if funded Plan on initiating a new IACUC application if funded IACUC approval is not needed for the proposed work
Please explain why IACUC approval is not needed for project involving live vertebrates.
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IACUC Number
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Budget Justification (1 page max)
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Biosketch for [pi_name]
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Biosketch for ______
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Biosketch for ______
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Biosketch for ______
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Biosketch for ______
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Biosketch for ______
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Biosketch for ______
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Biosketch for ______
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Biosketch for ______
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Biosketch for ______
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Letter(s) of Support, if needed
Other Supporting Documentation, if needed
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