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Rhode Island Hospital Injury Control COBRE
Funding Opportunities
The Rhode Island Hospital (RIH) Injury Control COBRE is pleased to announce two funding opportunity for injury control research.
About RIH Injury Control COBRE
The RIH Injury Control COBRE brings together junior investigators, senior faculty and advisory committee members to build a center which produces high level, independent researchers equipped to address and improve the substantial burden of injury on population health. The RIH Injury Control COBRE is made up of an Administrative Core, Injury Control Digital Innovation Core & Injury Control Research to Practice and Policy Core needed to develop and sustain a thematic multidisciplinary center of research excellence on injury control. The Injury Control Digital Innovation Core (1) provides a scientifically rigorous structure that facilitates the development and evaluation of innovative digital health-based injury control, through expert consultation on qualitative research, analysis of big data and study design; (2) facilitates partnerships between researchers, clinicians, at-risk populations and relevant industry-based partners, with a focus on enhancing quality and dissemination of research and (3) develops and maintains an “innovation lab” of asynchronous and real-time injury-focused digital health training resources for junior researchers. The Injury Control Research to Practice and Policy Core (1) provides a robust infrastructure of methodologic support to facilitate injury control research moving forward into clinical practice and policy and (2) creates systems to train injury control researchers to rapidly and effectively disseminate research findings with the goal of impacting clinical practice and policy. The RPP Core inspires innovation in translational research, promoting interdisciplinary collaborations among technology professionals, scientists, clinicians, community members, and stakeholders.
Each pilot project and research project leader project must align with the COBRE research core priorities and can address any component of injury control (injury prevention, treatment or rehabilitation). The Injury Control COBRE is committed to recruiting and retaining research led by and serving racial and ethnic minorities.
A Pilot Leader must hold a faculty appointment at the time that the award is made. Faculty investigators at any rank (includes established investigators) are allowed to lead Pilot Projects, however, junior investigators with research-, or clinical-track faculty appointments will be given priority. Individuals holding postdoctoral training positions are not eligible to lead Pilot Projects. The junior investigator is defined either as (1) an individual who does not have and has not previously had an external, peer-reviewed research project grant (R01) or Program Project Grant (PPG) from either a Federal or non-Federal source that names that investigator as the PD/PI, or an established investigator who is making a significant change to his/her career focus.
Grants that name an applicant as a co-investigator, collaborator, consultant, or a position other than PD/PI, do not disqualify the applicant. Academic Research Enhancement Award (AREA) grants, exploratory/pilot project grants (such as NIH R03 and R21 awards), mentored career development awards (such as NIH K01 and K08 awards), or other Federal or non-Federal funding whose purpose is to provide preliminary support in anticipation of an RPG or PPG also do not disqualify the applicant.
Investigators must have a research mentor in a field related to the proposed research. If needed, the Injury Control COBRE Executive Committee can help investigators identify an appropriate research mentor. Contact COBRE Administrator Julie Bromberg at jbromberg@brownhealth.org for more information.
Funding is offered for each pilot project for up to 2 years with a total budget of up to $50,000 direct costs. Indirect costs will not be provided to the applicants’ home institution.
The Budget may include federally allowable research expenses and supplies. Equipment cannot be purchased. Awards are not transferrable in the event the Pilot Project Leader transfers to a non-eligible institution. Unused funds revert to the COBRE.
The project duration is up to 24 months. A progress report will be submitted with the COBRE annual reporting to NIH/NIGMS in the RPPR report. Second year of funding is dependent upon a successful completion of year one objectives.
Application Process
Letter/Presentation of Intent
All applicants must submit a Letter of Intent or a Presentation on Intent. Letters should be submitted to Julie Bromberg at jbromberg@brownhealth.org. If you prefer to give a presentation, please email Julie Bromberg to schedule a virtual presentation. COBRE Faculty are available to meet with applicants to discuss how to strengthen your Letter/Presentation of Intent. Contact Julie Bromberg to connect with COBRE faculty.
Materials should include:
Letters/Presentations of Intent will be reviewed to ensure eligibility and that the proposed research fits with the mission of the COBRE. Selected applicants will be invited to submit a full proposal. Those invited to submit a full proposal will be asked to discuss their proposal with the Injury Control COBRE Core Directors.
Applications will follow abbreviated NIH format using PHS 398 forms with minor modifications. See checklist for a complete list of application components. Applicants should work with their departmental grant administrator to be sure the application complies with COBRE and NIH rules. Also please note the following:
Additional Requirements
All COBRE funded investigators are required to adhere to NIGMS directives. Specifically, NIH funds may not be used to support any Diversity Equity and Inclusion related activities, or for any DEI-related research or training activities, or programs. A term and condition to this effect will be included in any Notice of Grant Award. In addition, NIH funds may not be used to support research activities involving climate change, vaccine hesitancy, gender identity, or collaborations with China. If this award involves human subjects research, information regarding study participant “gender” should not be collected. Rather, “sex” should be used for data collection and reporting purposes.
All COBRE funded investigators are required to participate in a number of technical assistance activities/services with the goal of submitting for additional funding in your injury control research area by study completion including:
Please use this checklist to assure your PPL application is complete. Contact Julie Bromberg with any questions or concerns.
Coordinate with your Departmental Administrator to complete/ approve your application. | ||||
NIH Face Page (PHS 398 Form 1) | ||||
Project Summary (PHS 398 Form 2) | 30 lines | |||
Specific Aims | 1 page | |||
Research Strategy | 6 pages | |||
Bibliography | -- | |||
Budget | -- | |||
Budget Justification | -- | |||
Subcontract Budget (if applicable) | -- | |||
Subcontract Budget Justification (if applicable) | -- | |||
Biosketches (Key Personnel, Other Significant Contributors, Consultants) | 5 pages each | |||
CITI Training documentation for PI/Research Staff | ||||
IRB Submission Documentation (pending approval is acceptable) | ||||
Required for research involving human subjects (not a clinical trial): | ||||
Human Subject Information (PDF Form) - Sections 1 - 3 required (leave Section 4 blank) | -- | |||
Inclusion of Individuals Across the Lifespan | ||||
Inclusion of Women, Minorities and Children | -- | |||
Recruitment & Retention Plan | -- | |||
Inclusion Enrollment Table | ||||
Protection of Human Subjects | -- | |||
Data Safety Monitoring Plan (this is optional) | ||||
Study Timeline (this is optional) | -- | |||
Commitment to Technical Assistance Activities Letter | ||||
Required for NIH defined clinical trials: | ||||
Human Subject Information (PDF Form) - Sections 1 - 4 required | -- | |||
Inclusion of Individuals Across the Lifespan | ||||
Inclusion of Women, Minorities and Children | -- | |||
Recruitment & Retention Plan | -- | |||
Study Timeline | -- | |||
Inclusion Enrollment Table | ||||
Protection of Human Subjects | -- | |||
Data Safety Monitoring Plan | -- | |||
Overall Structure of Study Team | -- | |||
Statistical Design & Power | -- | |||
Dissemination Plan | -- |
Eligibility
The Research Project Leader must be employed in Rhode Island, with priority given to those based at Rhode Island Hospital/ Hasbro Children’s Hospital. Postdoctoral fellows or other positions that do not carry independent faculty status (or equivalent) will disqualify that individual and his/her research project from further consideration, unless evidence is provided that a faculty appointment is forthcoming prior to approval by NIGMS.
A junior investigator who does not have and has not previously been a PI on an external, independent, peer-reviewed research project grant (R01) or Program Project Grant (PPG) or PPG subproject, or equivalent award from either a Federal or non-Federal source.
Although priority is given to early career investigators, an established investigator who is making a significant change to his/her career goals by initiating a new line of research that is distinctly and significantly different from his/her current investigative program may also serve as a Research Project Leader.
The intent of this FOA is to support and develop promising investigators whose early career support consists of awards geared toward initiating their intended area of research. Each Research Project Lead should indicate in his/her Biographical Sketch their current and previous history of peer-reviewed research support.
Foreign components are not allowed.
Special Considerations
While the best science will be prioritized and the ability of the investigator to contribute to and meet the goals of the Center, special consideration will be given to those who (in no particular order):
Funding Available & Use of Funds
Application budgets may not exceed $150,000 in direct costs per year.
Faculty effort must be a minimum of 6 calendar months. Salary for technical personnel are permissible. Costs for equipment (>$1,000 per item) require prior approval. Renovation and/or honorariums are not allowed. Computer Support fees are not allowable.
All regulatory approvals (NIGMS, IRB, COBRE External Advisory Committee) must be obtained before funding is made available to your institution.
Unused funds will be deobligated and revert to the COBRE. COBRE Research Project awards are NOT transferable to institutions outside of Rhode Island. If the Principal Investigator transfers to a non-eligible institution, the remaining project grant funds will be deobligated back to the COBRE.
Performance Period
The funding period is 2 years (or until R01 level funding is secured) with potential for a third year of funding pending review, approval, and the availability of funds. A progress report will be submitted with the COBRE annual reporting to NIGMS in the RPPR report. Continued funding is dependent upon a successful completion of annual objectives.
Letter/Presentation of Intent
All applicants must submit a Letter of Intent or a Presentation of Intent. Letters should be submitted to Julie Bromberg at jbromberg@brownhealth.org . If you prefer to give a presentation, please email Julie Bromberg to schedule a virtual presentation. COBRE Faculty are available to meet with applicants to discuss how to strengthen your Letter/Presentation of Intent. Contact Julie Bromberg to connect with COBRE faculty.
Materials should include:
Letters/Presentations of Intent will be reviewed to ensure eligibility and that the proposed research fits with the mission of the COBRE. Selected applicants will be invited to submit a full proposal. Those invited to submit a full proposal will be asked to discuss their proposal with the Injury Control COBRE Core Directors.
Full Proposal
Using PHS398 forms and instructions, applications should use standard NIH formatting requirements (½ inch margins, Arial size 11-point font). The full application should be submitted via Piestar RFx. See checklist on last page for a complete list of application components. Applicants should work with their departmental grant administrator to be sure the application complies with COBRE and NIH rules. Also please note the following:
Review Process and Selection Criteria
Applications will be reviewed by the Injury Control COBRE Executive Committee. Recommendations will be provided to the COBRE’s External Advisory Committee and to the NIGMS for final determination. Applications will be evaluated using NIH scoring for scientific merit including significance, investigators, innovation, and approach. Reviews will also assess the proposal’s relevance to the long-term objectives of the Injury Control COBRE, proposed interaction with Injury Control COBRE Cores and potential for future independent funding. Funding is dependent upon the final approval of the NIGMS.
Regulatory Approvals
If your project includes human subjects or vertebrate animals, institutional IRB or IACUC (respectively) approval is required before the proposal can forwarded to NIH for final approval/ release of funds.
Additional Requirements
All COBRE funded investigators are required to adhere to NIGMS directives. Specifically, NIH funds may not be used to support any Diversity Equity and Inclusion related activities, or for any DEI-related research or training activities, or programs. A term and condition to this effect will be included in any Notice of Grant Award. In addition, NIH funds may not be used to support research activities involving climate change, vaccine hesitancy, gender identity, or collaborations with China. If this award involves human subjects research, information regarding study participant “gender” should not be collected. Rather, “sex” should be used for data collection and reporting purposes.
All COBRE funded investigators are required to participate in a number of technical assistance activities/services with the goal of submitting for additional funding in your injury control research area by study completion including:
Milestones
Research Project Leaders are expected to have submitted:
RPL Checklist
Please use this checklist to assure your RPL application is complete. Contact Julie Bromberg with any questions or concerns.
Coordinate with your Departmental Administrator to complete/approve your application. | ||||
NIH Face Page (PHS 398 Form 1) | ||||
Project Summary (PHS 398 Form 2) | 30 lines | |||
Project Narrative | 3 sentences | |||
Specific Aims | 1 page | |||
Research Strategy | 6 pages | |||
Bibliography |
| |||
Budget |
| |||
Budget Justification |
| |||
Checklist Format Page with F&A cost breakdwon |
| |||
Subcontract Budget (if applicable) |
| |||
Subcontract Budget Justification (if applicable) |
| |||
Biosketches (Key Personnel, Other Significant Contributors, Consultants) | 5 pages each | |||
NIH Other Support Form |
| |||
Mentor(s) Letter(s) of Support |
| |||
Departmental Chair Letter of Support |
| |||
CITI Training documentation for PI/Research Staff |
| |||
IRB Submission Documentation (pending approval is acceptable) |
| |||
Commitment to Technical Assistance activities letter |
| |||
Required for research involving human subjects (not a clinical trial): |
| |||
Human Subject Information (PDF Form) - Sections 1 - 3 required (leave Section 4 blank) |
| |||
Inclusion of Individuals Across the Lifespan |
| |||
Inclusion of Women, Minorities and Children |
| |||
Recruitment & Retention Plan |
| |||
Inclusion Enrollment Table |
| |||
Protection of Human Subjects |
| |||
Data Safety Monitoring Plan (this is optional) |
| |||
Study Timeline (this is optional) |
| |||
Required for NIH defined clinical trials: |
| |||
Human Subject Information (PDF Form) - Sections 1 - 4 required |
| |||
Inclusion of Individuals Across the Lifespan |
| |||
Inclusion of Women, Minorities and Children |
| |||
Recruitment & Retention Plan |
| |||
Study Timeline |
| |||
Inclusion Enrollment Table |
| |||
Protection of Human Subjects |
| |||
Data Safety Monitoring Plan |
| |||
Overall Structure of Study Team |
| |||
Statistical Design & Power |
| |||
Dissemination Plan |
|