RFA-ES-27-004-Full-Announcement.html
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- Opportunity number
- RFA-ES-27-004
About this file
This is a Request for Application (RFA) announcing the Limited Competition: Superfund Hazardous Substance Research and Training Program (P42 Clinical Trial Optional) under the National Institute of Environmental Health Sciences (NIEHS). The program supports problem-based, solution-oriented research centers addressing hazardous substances at Superfund sites through integrated biomedical research (BMR) and environmental science and engineering (ESE) projects. Eligible applicants are limited to accredited institutions of higher education, though subcontracts with other organizations are permitted. The RFA prioritizes research addressing four mandates: advanced detection and assessment techniques for hazardous substances; risk assessment methods; environmental detection technologies; and biological, chemical, or physical methods to reduce contaminant toxicity and amount. Applications may request up to $1.75 million in direct costs annually for project periods up to five years, with NIEHS intending to fund approximately 10 awards totaling approximately $22 million for fiscal year 2027.
All applications must follow Multi-Project (M) instructions and include required components: an Administrative Core (providing leadership, data management, and training coordination); a Translational Research and Engagement Core (TREC) facilitating stakeholder engagement and research translation; a minimum of three research projects (with minimum one BMR and one ESE project, maximum two of each type); and optional Research Support Core for centralized services. The application deadline is September 25, 2026, with scientific merit review in March 2027, advisory council review in May 2027, and earliest start date of July 2027. Applications must be submitted through NIH ASSIST or institutional system-to-system solutions via Grants.gov; applicants must maintain active registrations in SAM, obtain a UEI, register with eRA Commons, and ensure all PDs/PIs have ORCID IDs. The RFA mandates substantial documentation including center organizational structure diagrams, integration tables, end-user stakeholder matrices, and data management and sharing plans, with emphasis on demonstrating multidisciplinary integration and relevance to EPA and ATSDR end-users.
RFA-ES-27-004-Full-Announcement.html
Text of this file
Department of Health and Human Services
Part 1. Overview Information
Participating Organization(s)
National Institutes of Health (NIH)
Components of Participating Organizations
National Institute of Environmental Health Sciences (NIEHS)
Funding Opportunity Title
Limited Competition: Superfund Hazardous Substance Research and Training Program (P42 Clinical Trial Optional)
Activity Code
P42 Hazardous Substances Basic Research Grants Program
Announcement Type
Reissue of
RFA-ES-23-001
Related Notices
| Check for any recent Notices of NIH Policy Changes that may impact application requirements. |
| January 23, 2026 - NIH Pause on New Submissions to the NIH Human Embryonic Stem Cell Registry and Request for Information on Reducing Reliance on Human Embryonic Stem Cells in NIH-Supported Research. See Notice NOT-OD-26-031. |
Funding Opportunity Number (FON)
RFA-ES-27-004
Companion Notice of Funding Opportunity
None
Number of Applications
Only one application per institution is allowed, as defined in Section III. 3. Additional Information on Eligibility. See Section III. 3. Additional Information on Eligibility.
Assistance Listing Number(s)
93.143
Notice of Funding Opportunity Purpose
The National Institute of Environmental Health Sciences (NIEHS) is announcing the continuation of the Superfund Hazardous Substance Research and Training Program, referred to as Superfund Research Program (SRP) Centers. SRP Center grants will support problem-based, solution-oriented research Centers that consist of multiple, integrated projects representing both the biomedical and environmental science and engineering disciplines; as well as cores tasked with administrative (which includes Center leadership, data management, and training); translational research and engagement; and research support functions. The scope of the SRP Centers is taken directly from the Superfund Amendments and Reauthorization Act of 1986, which limits competition for this program to accredited institutes of higher education.Please see Section III. Eligibility for additional information. In accordance with NIH standard peer-review processes, the application(s) will be peer-reviewed, and only meritorious application(s) will be considered for funding.
Funding Opportunity Goal(s)
To support innovative research and training through multi-project, interdisciplinary grants. Areas of research may include: (1) advanced techniques for the detection, assessment, and evaluation of the effects of hazardous substances on human health; (2) methods to assess the risks to human health presented by hazardous substances; (3) methods and technologies to detect hazardous substances in the environment; and (4) basic biological, chemical, and physical methods to reduce the amount and toxicity of hazardous substances.
Key Dates
Posted Date
May 19, 2026
Open Date (Earliest Submission Date)
June 01, 2026
The following table includes NIH standard due dates marked with an asterisk.
| Application Due Dates |
| Review and Award Cycles |
| New |
| Renewal / Resubmission / Revision (as allowed) |
| AIDS - New/Renewal/Resubmission/Revision, as allowed |
| Scientific Merit Review |
| Advisory Council Review |
| Earliest Start Date |
September 25, 2026 *
September 25, 2026 *
Not Applicable
| March 2027 | |
| May 2027 |
July 2027
September 25, 2027 *
September 25, 2027 *
Not Applicable
| March 2028 | |
| May 2028 |
July 2028
September 25, 2028 *
September 25, 2028 *
Not Applicable
| March 2029 | |
| May 2029 |
July 2029
All applications are due by 5:00 PM local time of applicant organization.
Applicants are encouraged to apply early to allow adequate time to make any corrections to errors found in the application during the submission process by the due date.
No late applications will be accepted for this Notice of Funding Opportunity (NOFO).
Expiration Date
September 26, 2028
Due Dates for E.O. 12372
Not Applicable
Required Application Instructions
It is critical that applicants follow the Multi-Project (M) Instructions in the How to Apply - Application Guide, except where instructed to do otherwise (in this NOFO or in a Notice from the NIH Guide for Grants and Contracts). Conformance to all requirements (both in the How to Apply - Application Guide and the NOFO) is required and strictly enforced. Applicants must read and follow all application instructions in the How to Apply - Application Guide as well as any program-specific instructions noted in Section IV. When the program-specific instructions deviate from those in the How to Apply - Application Guide, follow the program-specific instructions. Applications that do not comply with these instructions may be delayed or not accepted for review.
| There are several options available to submit your application through Grants.gov to NIH and Department of Health and Human Services partners. You must use one of these submission options to access the application forms for this opportunity. | |
| Use the NIH ASSIST system to prepare, submit and track your application online. | |
| Use an institutional system-to-system (S2S) solution to prepare and submit your application to Grants.gov and eRA Commons to track your application. Check with your institutional officials regarding availability. |
Table of Contents
Part 1. Overview Information Key Dates Part 2. Full Text of Announcement Section I. Notice of Funding Opportunity Description Section II. Award Information Section III. Eligibility Information Section IV. Application and Submission Information Section V. Application Review Information Section VI. Award Administration Information Section VII. Agency Contacts Section VIII. Other Information
Part 2. Full Text of Announcement
Section I. Notice of Funding Opportunity Description
Research Objectives The NIEHS invites qualified investigators from domestic institutions of higher education to submit an application for an SRP Center grant. SRP legislation, under SARA of 1986, allows NIEHS the flexibility to create university-based Centers to conduct research to address the wide array of scientific uncertainties facing the national Superfund program. Per 42 USC 9660 (a)(3) eligible applicants are limited to accredited institutes of higher education. Please see Section III. Eligibility for additional information. In accordance with NIH standard peer-review processes, the application(s) will be peer-reviewed, and only meritorious application(s) will be considered for funding. The complex problems related to sites impacted by hazardous substances requires the expertise of both biomedical research (BMR) and environmental science and engineering (ESE) disciplines. Applicants responding to this Notice of Funding Opportunity Announcement (NOFO) are expected to design a research Center that integrates BMR (e.g., toxicology, epidemiology, mechanistic studies) with ESE (e.g., remediation, geosciences, ecological sciences). The goal of a NIEHS SRP Center is to improve public health by supporting integrative, multidisciplinary research incorporating the following: responsiveness to mandates; problem-based, solution-oriented research; relevance to SRP and Superfund.
Responsiveness to Mandates: SARA Section 311(a) “Hazardous Substances Research and Training,” authorizes NIEHS to create a basic research and training program for the development of:
1) advanced techniques for the detection, assessment, and evaluation of the effect of hazardous substances on human health;
2) methods to assess the risks to human health presented by hazardous substances;
3) methods and technologies to detect hazardous substances in the environment; and
4) basic biological, chemical, and physical methods to reduce the amount and toxicity of hazardous substances.
To accomplish these mandates, Centers are expected to assemble interdisciplinary research teams with expertise in BMR and ESE to advance scientific knowledge using innovative and integrated approaches. Moreover, the SRP's fourth mandate reinforces the program's problem-solving mission; whereby, the research generated by SRP Centers would lead to strategies to prevent exposure and improve public health. Centers are also expected to facilitate transfer of research findings through coordinated data management and analysis; engage communities, end-users, and stakeholders with prevention/intervention strategies to reduce exposures; share findings to broader audiences; and train the next generation of scientists. (SRP defines stakeholders as those individuals and entities that benefit from SRP research and technologies in improving public health.)
Problem-based, Solution-oriented Research: Applicants are expected to design Centers that will contribute to solving a scientific problem(s) related to SRP’s mandates and with relevance to Superfund. The problem being solved could be a discreet but critical gap in the larger context of a complex issue, or it may answer a specific question, that if left unanswered, would create an impediment to effectively protect public health.
Relevance to SRP Mandates and Superfund: Given SRP’s broad mandates, it is important for interdisciplinary teams to work together to foster research that addresses Superfund relevant exposure pathways. Ultimately, problem-solving research seeks to find answers to inform real-life exposures – both in terms of understanding health implications as well as developing remedies for these exposures. For these reasons, applicants should assemble teams that consider multiple vantage points to address research challenges within a given mandate area, contaminant, or exposure scenario that may have the greatest potential for supporting the SRP's goal of protecting human health and the environment from the impact of hazardous substances.
The SRP also considers the diverse research and information needs of its end-users as important criteria for determining relevance. SRP end-users include the Superfund programs at the U.S. Environmental Protection Agency (EPA) and Agency for Toxic Substances and Disease Registry (ATSDR). In addition, U.S. Geological Survey (USGS), U.S. Department of Defense (DOD), and the U.S. Department of Energy (DOE) are important end-users of research and technology to manage and mitigate sites impacted by hazardous substances. In addition, the National Science Foundation (NSF) and other NIH Institutes and Centers may provide valuable opportunities to promote and leverage the findings of SRP research. The SRP also considers other federal, state, local, and Tribal governments, and communities impacted by hazardous substances as important end-users. Other stakeholders to be considered include formal/informal educational groups, hazardous waste practitioners, the general public, and other academic researchers. Therefore, investigators should seek input from end-users mentioned above during application development and identify critical issues for which fundamental science is needed.
(Note: Applications lacking clear relevance to SRP Mandates and Superfund will be considered nonresponsive.)
Center Structure To achieve a broad and sustained impact, SRP Centers are expected to include the following:
Administrative Core: an Administrative Core is required in each SRP Center grant application (which includes Center leadership, data management, and training functions):
| This Core provides leadership to the Center, maintains the organization of the Center, and ensures that the projects and cores are being supported to achieve the Center’s goals. |
| To support the NIH data sharing policy, the Administrative Core and its Data Management Coordinator are tasked with leveraging institutional/computing infrastructure to support the management and integration of data assets across the Center. They are expected to work closely with project/core leaders to ensure high data quality throughout the entire lifecycle of the data and identify opportunities for integrating project/core-generated data with other existing datasets, accelerating the impact of the Center's research. |
| The Administrative Core should include a Training Coordinator to promote scientific workforce development and provide opportunities to enhance the Center's graduate and postdoctoral trainees multi-disciplinary research experiences and training. For instance, trainees pursuing degrees in the environmental science and engineering areas should be encouraged to understand how their research fits into the context of biomedical research and vice versa for biomedical research-focused trainees. (Note: Per its mandates, the SRP defines "trainees" as graduate level training (e.g., Masters, PhD., Post doc). |
Translational Research and Engagement Core: a Translational Research and Engagement Core (TREC) is required in each SRP Center grant application. In support of the NIEHS Strategic Plan and its cross-cutting themes, SRP values not only solutions-focused research, but also its translation to enable health promotion, disease prevention, and evidence-based intervention. This is accomplished through two key core activities:
| Translational Research – The TREC will coordinate with each research project to explore translational research opportunities appropriate for the stage and type of science, identifying opportunities to move science across the research continuum, linking with potential stakeholders/end-users of the research results, and tailoring communication strategies for various audiences. |
| Stakeholder Engagement – The TREC is also expected to develop plans for the Overall Center’s multi-directional engagement with key partners, with the ultimate goal of enabling impacted communities and other stakeholders to be participants in the reduction of the amount and toxicity of hazardous substances in their environment (i.e., SRP's fourth mandate). |
Research Projects: Collectively, the Center's research projects (consisting of biomedical research projects and environmental science and engineering research projects) should represent a range of basic and applied research that contributes to the problem-based, solution-oriented goal of the Center. Projects should be hypothesis-driven or product-oriented research.
| Biomedical Research (BMR) Projects: A minimum of one (maximum of two) BMR projects are required and should address biomedical or human health-related implications of hazardous substances. This includes, but is not limited to, toxicology studies, epidemiology, mechanistic studies, genetic susceptibility, computational toxicology, biomedical engineering, preclinical/clinical intervention, or efficacy of prevention studies. |
| Environmental Science and Engineering (ESE) Projects: A minimum of one (maximum of two) ESE projects are required and should address environmental science or engineering implications of hazardous substances. These projects are integral to the protection of human health through predicting, detecting, and preventing exposures. At least one ESE project should support SRP’s fourth mandate “basic biological, chemical, and physical methods to reduce the amount and toxicity of hazardous substances.” ESE projects include, but would not be limited to: remediation, geochemistry, ecology, civil/environmental engineering, geology, microbiology, fate and transport, hydrogeology, and detection sciences. |
(Note: Centers should be comprised of a minimum of 3 (maximum of 4) Research Projects and could be a combination of 2 BMR/2 ESE or 2 BMR/1 ESE or 1 BMR/2 ESE.)
Research Support Core (Optional): Applicants may include a Research Support Core (RSC) to provide centralized resources/services in support of the scientific goals of at least two projects. This may include, but would not be limited to, analytical services, biostatistics, bioinformatics, geographical information systems, data visualization, and computational modeling, etc.
Integration: The SRP considers integration of a Center's projects and core as an important way to target complex problem(s) relevant to the SRP's mandates. A Center should demonstrate evidence of synergy between its projects and core - including interaction between BMR and ESE disciplines.
Scope of the SRP Center Grant The scope of the SRP Center is defined by the SRP Mandates. Research and supporting activities under this NOFO may utilize a variety of approaches to achieve SRP mandates, listed here:
1) Advanced techniques for the detection, assessment, and evaluation of the effect of hazardous substances on human health.
| Mechanistic and/or mode of action research that includes laboratory- and population-based (i.e. epidemiology) studies for unraveling critical biological pathways that contribute to disease when perturbed by environmental contaminants. |
| Molecular, genetic, epigenetic, and biochemical research that describe the normal physiological events and processes that contribute to good health and the roles that hazardous substances play in their disruption and progression of disease. |
| Cumulative impacts of combined exposures to hazardous substances and how they interplay with biological responses and host factors (e.g., nutrition, co-morbid disease/conditions, lifestyle habits, psychosocial stressors; genetic variability, epigenetic factors, sex, age, timing of exposure, resilience, and allostatic load) that impact disease susceptibility. |
| Application of novel and advanced tools and methods such as high-throughput screening techniques, “multi-omics” approaches, next generation sequencing, New Approach Methodologies (NAMs), tissue engineering (including organotypic tissues), in silico modeling, multi-scale modeling, artificial intelligence/machine learning, and systems biology approaches to improve predictive capabilities and characterize health effects. |
| Discovery and validation of technologies useful for exposure assessment, indicators of biological response (e.g., biomarkers of exposure and disease), and disease susceptibility. |
2) Methods to assess the risks to human health presented by hazardous substances.
| Integrated human and ecologic risk models to assist in making cost-effective and protective recommendations. |
| Novel methods/approaches/statistical/combinatorial models to integrate exposure over time, determining windows of susceptibility (e.g., early life and childhood exposures), and characterizing the attributable risk from multiple exposures experienced over one’s lifetime that result in chronic disease. |
| Methods that include incorporation of the exposome; microbiome; genetic variations (e.g., somatic mutations); adverse outcome, causal, and other pathway modeling; and macromolecular alterations (e.g., epigenetics) to identify susceptibility or resilience factors. |
| Exposure science research such as: fate and transport; transformation of contaminants in the environment; contaminant bioaccessibility/bioavailability in the environment and in biological systems; biological response indicators (e.g., biomarkers); factors that influence biological susceptibility/resilience (e.g. inflammation status); and quantifying body burden. |
3) Methods and technologies to detect hazardous substances in the environment.
| Development and application of new and advanced technologies for detection and monitoring of hazardous substances. |
| Development of novel methods and devices that offer precise and low-cost measuring capabilities of hazardous substances (e.g., bioassays or ecological indicators that assess toxicity to biological systems at sites complicated by multiple contaminant streams or complex environmental media). |
| Innovative tools that allow for real-time, minimally invasive, on-site monitoring. |
| Devices that are capable of multi-analyte readings and/or determination of the degree of bioaccessibilty/bioavailability of a contaminant (e.g., model organisms, passive sampling devices). |
| Technologies and methodologies that confer practical advantages over existing technologies (e.g., low-cost, user-friendly, readily accessible, and easily deployable for environmental disaster response) as well as device reuse, waste generation, and utilization of non-toxic components (particularly for in-situ devices). |
4) Basic biological, chemical, and physical methods to reduce the amount and toxicity of hazardous substances.
| Research investigating the mechanisms of nutrition, lifestyle, or other co-factors to mitigate toxicity and improve public health. |
| Technologies/approaches that reduce the amount and toxicity of hazardous substances. |
| Cost-effective technologies that reduce and/or eliminate contamination in media such as groundwater, sediments, fractured bedrock, soils, and/or drinking water. |
| Studies that validate or confirm risk reduction from prevention or intervention activities. |
| Research to understand how to effectively reduce the amount and toxicity of hazardous substances and any unintended toxicological consequences of a remediation technology. |
(Note: There is a requirement for Center applications to include at least one ESE project that supports Mandate #4.)
Examples of Research Topics: For a listing of research areas of interest to the SRP and its end-users, please refer to the Suggested Research and Activities document found on the SRP website.
Applicants are also encouraged to propose research that fills gaps or needs not currently addressed within the SRP. Applicants are also encouraged to review its list of current grant recipients.
Hazardous Substances: The following substances are relevant to SRP:
| Hazardous substances found at Superfund sites. Applicants may refer to the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) Priority List website for information on these hazardous substances. |
| Hazardous breakdown products of the above substances formed in environmental media by physical, chemical, or biological (e.g., plants, microorganisms) processes. |
| Hazardous metabolites of the above substances or their breakdown products formed after exposure to humans. |
The applicants should refer to the SRP's website for a list of hazardous substances, including emerging contaminants, that have been suggested for study by SRP end-users/stakeholders.
Applicants are strongly encouraged to consult with SRP staff for specific questions about the relevancy of a hazardous substance for this NOFO, as the presence of a compound on one of the lists mentioned above does not automatically make it relevant to the SRP. The SRP will place priority on research with a clear connection to understanding health effects relevant to populations living near or affected by sites impacted by hazardous substances. In addition, SRP encourages investigations on understudied chemicals found at Superfund sites to gain an understanding their health effects.
Although the SRP recognizes the important public health impact of research focusing on exposures to consumer product-related chemicals, non-point source air pollution, and non-point source water pollution, the SRP will place a higher priority on research with a clear connection to understanding exposures relevant to populations living near or affected by sites impacted by hazardous substances. Per SARA Mandates, hazardous substances do not include petroleum, natural gas, natural gas liquids, liquefied natural gas, or synthetic gas usable for fuel.
Activities on Hazardous Waste Sites The SRP is not a site-specific program; research activities proposed by the Center are not required to take place on Superfund or hazardous waste sites. However, whether through research project or core activity(ies), Centers are strongly encouraged to seek opportunities for interactions at Superfund sites, managed hazardous waste sites, and facilities where hazardous substances are located, which greatly increases the positive impact of SRP research and its utility to end-users. Superfund sites serve as a good conceptual model for research focusing on hazardous substances. (Note: The SRP is a research program, and activities that propose preliminary site assessment activities may not be considered responsive.) If on-site activities will be conducted, researchers must coordinate with appropriate federal/state/local/Tribal agencies and site officials in the early stages of project development and throughout the process. They should also observe best safety practices and include a process and timeline for reporting results. When applicable, applicants must:
| Propose a procedure for coordinating and documenting site activities including record of the research conducted, sample collected, or translational/engagement activities; and |
| Delineate procedures for multi-directional communication and outcome reporting to appropriate site officials, site managers, and SRP staff at NIEHS. |
Links to end-user points of contact and suggestions for Hazardous Waste Site access are included on the following webpage (under Additional Resources).
Annual Meetings It is the intent of the NIEHS to hold annual SRP grant recipient meetings. It is anticipated that the location of the meeting site will rotate among the different grant recipients and Research Triangle Park, NC. For more information, see Section IV. Application and Submission Information.
Investigators proposing NIH-defined clinical trials may refer to the Research Methods Resources website for information about developing statistical methods and study designs.
See Section VIII. Other Information for award authorities and regulations.
Section II. Award Information
Funding Instrument
Grant: A financial assistance mechanism providing money, property, or both to an eligible entity to carry out an approved project or activity.
Application Types Allowed
New
Renewal
Resubmission
The OER Glossary and the How to Apply - Application Guide provides details on these application types. Only those application types listed here are allowed for this NOFO.
Clinical Trial?
Optional: Accepting applications that either propose or do not propose clinical trial(s).
Need help determining whether you are doing a clinical trial?
Funds Available and Anticipated Number of Awards
NIEHS intends to fund an estimate of up to 10 awards based on programmatic needs and availability of funds, corresponding to a total of up to approximately $22 million, for fiscal year 2027. Future year amounts will depend on annual appropriations.
Award Budget
Applications may request a budget for direct costs of up to $1.75 million dollars for each year.
Award Project Period
Applications may propose a project period of up to 5 years.
NIH grants policies as described in the NIH Grants Policy Statement will apply to the applications submitted and awards made from this NOFO.
Section III. Eligibility Information
1. Eligible Applicants
Eligible Organizations
| Higher Education Institutions - Includes all types | |
| Public/State Controlled Institutions of Higher Education | |
| Private Institutions of Higher Education |
Foreign Organizations/International Collaborations
Non-domestic (non-U.S.) Entities (Foreign Organization) are not eligible to apply.
Non-domestic (non-U.S.) components of U.S. Organizations are not eligible to apply.
Foreign components, as defined in the NIH Grants Policy Statement, are not allowed.
Required Registrations
Applicant organizations Applicant organizations must complete and maintain the following registrations as described in the How to Apply- Application Guide to be eligible to apply for or receive an award. All registrations must be completed prior to the application being submitted. Registration can take 6 weeks or more, so applicants should begin the registration process as soon as possible. Failure to complete registrations in advance of a due date is not a valid reason for a late submission, please reference NIH Grants Policy Statement Section 2.3.9.2 Electronically Submitted Applications for additional information.
System for Award Management (SAM) – Applicants must complete and maintain an active registration, which requires renewal at least annually. The renewal process may require as much time as the initial registration. SAM registration includes the assignment of a Commercial and Government Entity (CAGE) Code for domestic organizations which have not already been assigned a CAGE Code. Foreign organizations must obtain a NATO Commercial and Government Entity (NCAGE) Code (in lieu of a CAGE code) in order to register in SAM. Unique Entity Identifier (UEI)- A UEI is issued as part of the SAM.gov registration process. The same UEI must be used for all registrations, as well as on the grant application.
| eRA Commons - Once the unique organization identifier is established, organizations can register with eRA Commons in tandem with completing their Grants.gov registration; all registrations must be in place by time of submission. eRA Commons requires organizations to identify at least one Signing Official (SO) and at least one Program Director/Principal Investigator (PD/PI) account in order to submit an application. |
| Grants.gov – Applicants must have an active SAM registration in order to complete the Grants.gov registration. |
Program Directors/Principal Investigators (PD(s)/PI(s)) All PD(s)/PI(s) must have an eRA Commons account. PD(s)/PI(s) should work with their organizational officials to either create a new account or to affiliate their existing account with the applicant organization in eRA Commons. If the PD/PI is also the organizational Signing Official, they must have two distinct eRA Commons accounts, one for each role. Obtaining an eRA Commons account can take up to 2 weeks.
All PD(s)/PI(s) must be registered with ORCID. The personal profile associated with the PD(s)/PI(s) eRA Commons account must be linked to a valid ORCID ID. For more information on linking an ORCID ID to an eRA Commons personal profile see the ORCID topic in our eRA Commons online help.
Eligible Individuals (Program Director/Principal Investigator)
Any individual(s) with the skills, knowledge, and resources necessary to carry out the proposed research as the Program Director(s)/Principal Investigator(s) (PD(s)/PI(s)) is invited to work with his/her organization to develop an application for support.
For institutions/organizations proposing multiple PDs/PIs, visit the Multiple Program Director/Principal Investigator Policy and submission details in the Senior/Key Person Profile (Expanded) Component of the How to Apply - Application Guide.
2. Cost Sharing This NOFO does not require cost sharing as defined in the NIH Grants Policy Statement Section 1.2- Definitions of Terms.
3. Additional Information on Eligibility Number of Applications
Applicant organizations may submit more than one application, provided that each application is scientifically distinct.
The NIH will not accept duplicate or highly overlapping applications under review at the same time per NIH Grants Policy Statement Section 2.3.7.4 Submission of Resubmission Application. This means that the NIH will not accept:
A new (A0) application that is submitted before issuance of the summary statement from the review of an overlapping new (A0) or resubmission (A1) application.
A resubmission (A1) application that is submitted before issuance of the summary statement from the review of the previous new (A0) application.
An application that has substantial overlap with another application pending appeal of initial peer review (see NIH Grants Policy Statement 2.3.9.4 Similar, Essentially Identical, or Identical Applications).
Based on 42 USC 9660(a)(3) eligible applicants are limited to accredited institutes of higher education. Eligible applicants are permitted under the law, and encouraged by NIEHS, to subcontract as appropriate with other organizations as necessary to conduct portions of the research. Examples of other organizations may include generators of hazardous wastes; persons involved in the detection, assessment, evaluation, and treatment of hazardous substances; owners and operators of facilities at which hazardous substances are located; and/or State and local governments.
Section IV. Application and Submission Information
1. Requesting an Application Package The application forms package specific to this opportunity must be accessed through ASSIST or an institutional system-to-system solution. A button to apply using ASSIST is available in Part 1 of this NOFO. See the administrative office for instructions if planning to use an institutional system-to-system solution.
2. Content and Form of Application Submission It is critical that applicants follow the Multi-Project (M) Instructions in the How to Apply - Application Guide, except where instructed in this notice of funding opportunity to do otherwise (in this NOFO, in a policy notice, or other notice from NIH Guide for Grants and Contracts) and where instructions in the How to Apply - Application Guide are directly related to the Grants.gov downloadable forms currently used with most NIH opportunities. Conformance to the requirements in the How to Apply - Application Guide is required and strictly enforced. Applications that are out of compliance with these instructions may be delayed or not accepted for review.
Page Limitations All page limitations described in the How to Apply- Application Guide and the Table of Page Limits must be followed.
| Component |
| Component Type for Submission |
| Page Limit |
| Required/Optional |
| Minimum |
| Maximum |
| Overall |
| Overall |
| 12 |
Required
| 1 |
| 1 |
| Admin Core |
| Admin Core |
| 12 |
Required
| Translational Research and Engagement Core |
| TREC |
| 12 |
Required
| Research Project |
| Project |
| 12 |
Required
| Research Support Core |
| RSC |
| 6 |
Optional
Instructions for the Submission of Multi-Component Applications
The following section supplements the instructions found in How to Apply- Application Guide and should be used for preparing a multi-component application.
| Note for Research Projects: | |
| Biomedical Research Projects (BMR): required, minimum of 1; maximum of 2 | |
| Environmental Science and Engineering Research Projects (ESE): required, minimum of 1; maximum of 2 |
Centers must be comprised of a minimum of 3 (maximum of 4) Research Projects and could be a combination of 2 BMR/2 ESE or 2 BMR/1 ESE or 1 BMR/2 ESE.
Overall Component When preparing the application, use Component Type ‘Overall’.
All instructions in the How to Apply - Application Guide must be followed, with the following additional instructions, as noted.
SF424(R&R) Cover (Overall) Complete entire form.
PHS 398 Cover Page Supplement (Overall) Follow standard instructions.
Research & Related Other Project Information (Overall) Follow standard instructions.
| Project Summary/Abstract: For the Overall Component, applicants must include a Project Summary/Abstract that describes: | |
| The scientific problem(s)/overall hypothesis being addressed by the Overall Center and how the Center plans to solve these target problem(s) related to health effects, risk, detection and/or remediation of hazardous substances (i.e., with relevance to SRP mandates and Superfund). | |
| An overall indication of the importance of the proposed science and what the Center proposes to accomplish. | |
| Which hazardous substances are being evaluated, study sites, research approaches, model organisms/biological systems, disease pathways, etc. | |
| Aspects of the Center that are particularly innovative or paradigm-shifting. | |
| How the cores will be integrated into the Center. | |
| How the Center will reduce disease/dysfunction and improve public health. |
Project Narrative: It should be clear in the "Project Narrative" (i.e., the "public health relevance" statement) the relevance of the Center’s activities to public health, end-users/stakeholders, Superfund, and the SRP mandates.
Other Attachments: The following "Other Attachments" must be included with the overall component to aid in the review of applications. The filename provided for each attachment will be the name used for the bookmark in the application image.
| Center Organizational Structure. Applicants should include a diagram of the organizational structure of the Center. This diagram should demonstrate how the interactions between the different Center components achieve integration and the mandate-driven goals of the Center. List the names of the respective component leads (including the Administrative Core's Data Management and Training Coordinators as well as the TREC Coordinator(s)). Applicants should clearly indicate which projects are BMR and which are ESE. The diagram should be provided as a pdf file titled "Center Organizational Structure." | |
| Table of Integration with Center. To assist the reviewers in determining the relationship between components, a table should be provided showing interactions between projects and cores (by project title and project/core leader) and the purpose of the interaction for the achievement of the Center's overall objectives. This table should be provided as a pdf file titled "Table of Integration with Center." | |
| Table of End-users/Stakeholders and Field Sites. To assist the reviewers in identifying significant project and core interactions with key end-users/stakeholders and field sites, a table should be provided showing which projects and cores interact with which end-users, stakeholders, and field sites as well as the type of interaction/activity. End-users/stakeholders would include federal/state/local/Tribal agencies, community groups, community(ies), and other end-users with significant ongoing and/or planned interactions. Field sites would include Superfund, hazardous waste sites, facilities at which hazardous substances are located, or other study/research sites. This table should be provided as a pdf file titled "Table of End-users and Field Sites." | |
| For Renewal/Resubmissions: | Table of Changes to Projects and Cores. To assist review of renewal/resubmission applications, a table should be included that lists projects and core components (by project title and project/core leader/coordinator) denoting which projects are new, continuing, substantially modified, finished/completed, or discontinued. This table should coincide in order and number with the projects and cores in the current application. Also, the applicant should indicate which projects are considered biomedical research (BMR) and which are considered environmental science and engineering (ESE) research. Indicate which ESE project(s) supports Mandate 4. ASSIST assigns projects/cores consecutively; therefore, when numbering projects and cores, numbering must not be skipped if a project from a previous funding period is discontinued in the renewal application. Please label in the following format: new = N; continuing = C; substantially modified = M; finished/completed = F; or discontinued = D. This table should be provided as a pdf file titled "Table of Changes to Projects and Cores". |
Please refer to the following website for example illustrations of the tables.
Project/Performance Site Locations (Overall) Enter primary site only.
A summary of Project/Performance Sites in the Overall section of the assembled application image in eRA Commons compiled from data collected in the other components will be generated upon submission.
Research and Related Senior/Key Person Profile (Overall) Include only the Project Director/Principal Investigator (PD/PI) and any multi-PDs/PIs (if applicable to this NOFO) for the entire application.
A summary of Senior/Key Persons followed by their Biographical Sketches in the Overall section of the assembled application image in eRA Commons will be generated upon submission.
Budget (Overall) The only budget information included in the Overall component is the Estimated Project Funding section of the SF424 (R&R) Cover.
A budget summary in the Overall section of the assembled application image in eRA Commons compiled from detailed budget data collected in the other components will be generated upon submission.
PHS 398 Research Plan (Overall) Introduction to Application: For Resubmission and Revision applications, an Introduction to Application is required in the Overall component.
Specific Aims: Applicants must provide Specific Aims for the Overall Center describing the objectives and goals of the Center, as they relate to the SRP Mandates and Superfund. The Specific Aims section should provide greater scientific detail and approaches than the overall Summary/Abstract. In addition, it should be clear how the components of the Center will interact to solve the target scientific problem(s) proposed by the Center, and the role of each project and core in contributing to resolving the problem(s) stated in the application.
Research Strategy: The Research Strategy section should highlight the following subsections: Significance and Relevance to SRP Mandates and Superfund; Research Team; Innovation, Approach; Environment; and Center Integration. Descriptions should include:
Significance and Relevance to SRP Mandates and Superfund
| How the hazardous substance(s) being studied, and their subsequent research findings/results, are relevant to the SRP and Superfund. |
| The role that each project and core have in contributing to resolving the problem(s) related to health effects, risk, detection and/or remediation of hazardous. |
| Identifying where the research can make a big impact in reducing the prevalence and burden of disease/dysfunction from exposure to hazardous substances as well as an understanding of the molecular, cellular, and pathophysiologic parameters associated with these hazardous substances. |
| How the Overall Center is relevant to SRP’s end-users (e.g., the agencies responsible for management of sites impacted by hazardous substances, as well as the individuals and communities impacted by these sites) and other Center stakeholders (as applicable). |
| Information/data to assist risk assessors and remediation managers at sites impacted by hazardous substances. |
Research Team
| An introduction to the leadership and key personnel of the Center, highlighting the complementary and integrated expertise and breadth of disciplines among the project and core leaders/coordinators to accomplish the goals of the Center (without duplicating information in biosketches). |
| Outline, on a per project/core basis, the expertise associated with the hazardous substances being evaluated, and the capability of the research team to access study sites, conduct the research approaches, and knowledge of model systems/disease pathways, etc. |
| The successes and accomplishments of the team as a whole in advancing their respective field - particularly with regard to integration between disciplines. |
| A brief description of plans for the Administrative Core and the TREC (and RSC, if applicable) to facilitate the overall goals of the Center and maintain organization of the Center. |
Innovation, Approach, and Environment:
| The importance of the knowledge gap(s) the Center is fulfilling. |
| Novel theoretical concepts, approaches or methodologies, instrumentation, or interventions including novel adaptations of technologies from one field to another (i.e., multi-disciplinary approaches). |
| How the Center’s strategies ensure a robust, unbiased approach. |
| The degree to which the experimental design(s) recapitulate real world exposures. |
| How the university environment supports the Center's problem-solving goals (e.g., institutional support; and/or interdepartmental/interinstitutional cooperation). |
Center Integration:
| The multidisciplinary and interdisciplinary nature of the Center. |
| The integration and interactions between the BMR and ESE projects and between the various projects and the cores (i.e., the Administrative Core, TREC, and the RSC (if applicable)). |
| How each project and core contribute to the Center’s theme, and how the Overall Center is greater than the sum of its parts (i.e., components). |
(For Center integration, the applicant may also wish to cross-reference other sections of the application where more detailed information is found. For example, the Overall "Other Attachments" includes the “Center Organizational Structure”; “Integration with Center,” “End-users and Field Sites,” and “Changes to Projects and Cores” (as applicable). Other sections where interaction may be demonstrated include the Relation to Overall Center sections.)
For Renewal Applications. Renewal applications must include, in the Research Strategy, a general progress report that describes achievements under the grant since the last competitive review. The progress report should not be a copy of the material included for the individual projects. (The individual research projects/cores will also provide a “Progress Report” in their respective Research Strategy sections). Items to be included are the following:
| Brief summary of major accomplishments of the Center in achieving its problem-solving goals. |
| Brief highlights of integration and synergy among the projects and cores within the Center. |
| Brief report on projects and cores that are not being continued, and the reason for removing them from the Center. Be certain to reference relevant tables (e.g., "Table of Changes to Projects and Cores", described above). |
Timeline: Applicants should also provide an Overall Center timeline for the completion of problem-solving goals.
Letters of Support: Applicants should include all letters of support pertaining to the Overall Center in this section. For example, these letters may include collaborative agreements for the entire Center (e.g., from potential end-users/stakeholders), institutional support (if applicable), etc. However, only those Letters of Support that pertain to a specific project/core should be placed in the respective project/core. Applications that propose work with American Indian or Alaska Native populations, tribes or communities must include letters of support from the appropriate tribal officials and/or tribal organizations as applicable. See the Application Guide for instructions.
Resource Sharing Plan:
Individuals are required to comply with the instructions for the Resource Sharing Plans as provided in the How to Apply - Application Guide.
Other Plan(s):
All instructions in the How to Apply- Application Guide must be followed, with the following additional instructions:
A Data Management and Sharing Plan (DMS Plan) is required for any NIH-funded or conducted research that will generate scientific data. Applicants must submit the DMS Plan at the time of application using the NIH DMS Plan Format Page. The DMS Plan must address the elements in the structured format should not exceed two (2) pages. Where the DMS Plan Format Page requires a “Yes or No” response, no additional narrative is allowed. The Data Management and Sharing (DMS) Plan must be provided in the Overall component.
Appendix:
Only limited items are allowed in the Appendix. Follow all instructions for the Appendix as described in How to Apply- Application Guide; any instructions provided here are in addition to the How to Apply - Application Guide instructions.
PHS Human Subjects and Clinical Trials Information (Overall) When involving human subjects research, clinical research, and/or NIH-defined clinical trials follow all instructions for the PHS Human Subjects and Clinical Trials Information form in the How to Apply - Application Guide, with the following additional instructions:
If you answered “Yes” to the question “Are Human Subjects Involved?” on the R&R Other Project Information form, there must be at least one human subjects study record using the Study Record: PHS Human Subjects and Clinical Trials Information form or a Delayed Onset Study record within the application. The study record(s) must be included in the component(s) where the work is being done, unless the same study spans multiple components. To avoid the creation of duplicate study records, a single study record with sufficient information for all involved components must be included in the Overall component when the same study spans multiple components.
Study Record: PHS Human Subjects and Clinical Trials Information All instructions in the How to Apply - Application Guide must be followed.
Delayed Onset Study
Note: Delayed onset does NOT apply to a study that can be described but will not start immediately (i.e., delayed start). All instructions in the How to Apply- Application Guide must be followed.
PHS Assignment Request Form (Overall) All instructions in the How to Apply- Application Guide must be followed.
Administrative Core When preparing your application, use Component Type ‘Admin Core.’
All instructions in the SF424 (R&R) Application Guide must be followed, with the following additional instructions, as noted.
SF424 (R&R) Cover (Administrative Core) Complete only the following fields:
| Applicant Information |
| Type of Applicant (optional) |
| Descriptive Title of Applicant’s Project |
| Proposed Project Start/Ending Dates |
PHS 398 Cover Page Supplement (Administrative Core) Follow standard instructions.
Research & Related Other Project Information (Administrative Core) Human Subjects: Answer only the ‘Are Human Subjects Involved?’ and 'Is the Project Exempt from Federal regulations?’ questions.
Vertebrate Animals: Answer only the ‘Are Vertebrate Animals Used?’ question.
Project Summary/Abstract: Include a Core Summary/Abstract that briefly describes:
| How the Administrative Core will provide leadership and oversight to the Center and ensure that the Center’s BMR and ESE projects and TREC and RSC (if applicable) cores are being supported to achieve the Center’s goals. |
| Specific activities and innovative plans for supporting data management, which includes key activities that will be conducted by the Data Management Coordinator (e.g., how they will support the management and integration of data assets across the Center and how they will leverage institutional and computing infrastructure). |
| Specific activities for coordinating trainee activities for the projects and cores within the Center tailored to fit the overall goals of the Center, including how they will support the trainees' professional and multidisciplinary research experiences. |
Project Narrative: It should be clear in the "Project Narrative" (i.e., the "public health relevance" statement) the relevance of the Center’s activities to public health, end-users/stakeholders, Superfund, and the SRP mandates.
Other Attachments: Trainee List (For renewal applications only). Renewal applications must provide a "Trainee List".
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