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Tips & FAQ’s


Proposal Preparation Tips

Below is a consolidation of previously published NIH articles that discussed: the grant application process, useful advice and guidance for the preparation of a successful research application, factors that determine the scientific merit of a research application and other significant considerations.


Abstract

The abstract is one of the most neglected parts of the grant application. Although it should be written last, it needs to be written with care. The applicant should use the abstract to excite the reader's interest in the work. Keep in mind, this will very likely be the most widely read part of the application.

Budgets

Be honest. Some investigators may budget below their actual need in the belief that this improves their chances for funding. Reviewers have expert knowledge of the funds required to do research in the field. Underestimating your costs can be as damaging as inflating costs and putting in 'fat'. In many cases, it is wiser to calculate a real budget, and request that amount. Every item on the budget, particularly personnel, must be clearly justified.

Describe the role of all personnel, professional and nonprofessional, regardless of whether salary is requested. Specify each individual's unique qualifications and role in the project, including percent time (now expressed as months) and effort.

Thoroughly justify all proposed purchases of major equipment. If supplies appear unnecessary or redundant, they will most likely be disallowed.

Biographical Sketches

Biographical sketches should show the competence and availability of project personnel. Each sketch should include the individuals' publications in the past three years.

Resources and Environment

Facilities and equipment listed should be directly related to the project. Do not list or request equipment that, while state-of-the-art or a status symbol of the "well-stocked" laboratory, are unnecessary to the project. Demonstrate the quality of the institutional setting, staff, lab facilities and unique equipment. Also highlight involvement and collaboration with colleagues that would strengthen the project.

Research Plan

The research plan is the heart of the grant application. A good research plan is usually based on a meaningful hypothesis. The hypothesis should have a subset of specific project aims and scientific questions. The questions and aims, in turn, should have a focused subset of research methods to accomplish or answer them. A creative, exciting, and significant hypothesis is often the first step in a sound and well-received research plan; a sound research plan is necessary to a successful application.

The applicant, in describing their research plan, should not assume that the reviewer will "know what they mean." While the applicant may assume that the reviewers are experts in the field and up-to-date with current methodology, the reviewers will not make the same assumption of the investigator. In other words, the burden is on the applicant to clearly display their knowledge of methodology by detailing the specific experimental design, materials, techniques, and rational to accomplish the aims of the project.

While writing the entire proposal, but most crucially while developing the research plan, keep in mind the review criteria of the funding organization. The following mandated NIH research project review criteria, announced on May 5, 1997 by the NIH Peer Review Oversight Group, are applicable to most research proposals: 1) scientific, technical, or medical significance; 2) appropriateness and adequacy of experimental method; 3) innovative science; 4) qualifications of the PI and staff; and 5) availability of needed resources. Although these criteria may serve as a guideline, be aware of and address all review criteria of the funding organization, including such points as reasonableness of budget/research timeline and adequacy of human, animal, and environmental protections. These criteria are further detailed in the following discussion of the Research Plan sections.

This is also the section where the PI can demonstrate their knowledge and assessment of the relevant literature. This section should include a thorough, critically reviewed collection of data/events that justifies the next step: your current proposal.

The applicant may include preliminary studies published or in-press in the appendix to demonstrate the feasibility of the hypothesis and their qualifications as an investigator.

From this section, reviewers judge if the investigator understands the proposal's methodology and limitations. The experimental design, including technical methodology, should be mapped out clearly for each phase of the project. Each experiment should be tailored to a specific aim within the framework of the entire project. The framework of the project should include a realistic estimate of the work the PI can accomplish during each funding year requested. Justify as well as describe research designs and methods chosen and, if applicable, provide a comparison with alternative methods not chosen. If human or animal subjects are involved, address the characteristics of the subject population and evaluate the risk/benefit ratio. For animal subjects, indicate appropriate care before, during, and after the research period.

Describe the assumptions in the planned research. Along this line, mention likely potential limits or pitfalls and ways to work around such problems. This is particularly key should later experiments depend heavily on results from an initial phase of research.

Demonstrate appropriate and available controls, and a critical assessment of the proposed work. Define the criteria for evaluating whether a given test is a success or failure. Be certain to use correct statistical analyses if applicable. In some cases, the assistance of an expert statistician may be required for demonstrating proper statistical analyses in the proposal write-up, as well as providing assurance of proper statistical analyses of future research results.

Appendices

Appendices are useful for photographs, oversized documents, or other materials that do not reproduce well. The appendix can also include the PIs published manuscripts that are applicable to the proposal topic

General Tips

Read all instructions carefully and completely.

Good English

Good writing is vital to every proposal. In a period of increased competition and tight funding, the organized, well-written proposal will have the competitive edge over a poorly-written proposal of the same scientific merit. Some tips for clear, coherent scientific writing include:

As a general rule, write a thorough cohesive proposal, temporarily disregarding the page limits. If the first draft is too long, it should then be edited down to the allowed page limits. This allows the writer to better assess and prioritize the information (now compiled before them) to cut redundant or secondary information. In addition, this helps assure that the writer has not haphazardly omitted necessary information to stay within the prescribed page limits.

When complete, explanations should display thoroughness, clarity, AND brevity.

Seek Advice

The investigator should also allow time for pre-submission and review within their own organization. Peers in the scientific community can offer fresh perspectives or catch potential problems.
In addition, feel free to contact the Life Sciences Division proposal specialist or NIH staff for advice in preparing an application or clarifying questions.

Proofread the proposal before final submission

Allow extra time for thorough editing and proofreading of the proposal. A reviewer may assume a sloppy application reflects sloppy research, or lack of real concern in the funding of research. Proposals should be read for grammar, spelling, and typographical errors.

Avoid the Following

Frequently Asked Questions

Key Personnel

When should I list a person on my grant as key?

Key personnel are defined as, and should be limited to, individuals who contribute in a substantive way to the scientific development or execution of the project, whether or not salaries are requested. Typically, these individuals have doctoral or other professional degrees, although individuals at the masters or baccalaureate level should be included if their involvement meets the definition of key personnel.

Human and Animal Use Approvals

1. Who is responsible for getting Human Subjects and Animal Use Approval?

PIs are directly responsible for determining their own human subjects and animal use approval requirements. The assistance of Chris Byrne and Dianna Bolt in the Human and Animal Regulatory Committees (HARC) office at x5399 may be sought as needed. 

PIs are responsible for getting approval or exemption from further review for ALL projects involving human subjects and/or animal use, including projects using already approved protocols from other grants and projects where the actual animal work or human subjects interactions occur at another site. Researchers should bear in mind that human subjects approval may be required for projects using only human-derived DNA, cell lines, tissue cultures, and existing data. More complete definitions can be found on the HARC website (http://www.lbl.gov/ehs/health_services/harc/harc_intro.shtml) or in Chapter 22 of the Berkeley Lab Health and Safety Manual, Pub 3000. Departmental administrative staff  are often called upon to help PIs with the required paperwork. The following will provide a very brief overview of what is required.

2. When is human subjects or animal use approval required?

Separate human subject or animal use approval is required for each new experiment (protocol) and funding proposal. Annual renewal is required for all nonexempt protocols and proposals/projects. Funding may be interrupted for projects in which approval is allowed to lapse.
Human Subjects - Please note that if an exemption for human cell lines is granted, it is assigned to a proposal, not to the cell lines themselves. Thus every project using human cell lines requires approval. Once exempted, however, there is no requirement for annual review.
Animal use - Cell lines, or purchased animal tissue or products, are not subject to Animal Welfare regulations so do not require any kind of approval (ex: stock antibodies purchased from a chemical supplier). But research-derived tissues and antibodies which are custom made ARE considered animal use and require approval.

3. What is the approval process and timeline?

PIs are responsible for submitting the required paperwork to the HARC office in time to allow for appropriate review prior to the funding agency deadline; the HARC approval process takes up to eight weeks depending on the level of review required. HARC deadlines for given review dates are posted on their website. Evidence of approval of the project by the Berkeley Lab HARC is usually required by sponsors; please consult with your proposal specialist for filing guidance and agency deadlines. Note: NIH recently delayed review of a proposal for months when the required approval was not received by their deadline. Regardless of funding agency deadlines, approval must be in place before a new proposal is funded or work with human subjects or animals is begun.

4.  How do I get documentation of animal or human use approval for my grant?

The HARC office must compare new, competing, or modified grant proposals to the protocols identified by the researcher as covering the work.  Only after that review can the HARC office certify the proposal to Sponsored Projects and the sponsor.  This process is under review (Fall 2008) but current guidance can be found on line: Animal Welfare guidance /  Human Subjects guidance.

5. Where can I get the appropriate Human/Animal paperwork?

http://www.lbl.gov/ehs/health_services/harc/harc_intro.shtml

For clarification and more information, please review the HARC websites or contact Chris Byrne or Dianna Bolt in the HARC office, 486-5399 or harc@lbl.gov .

Links to More Q/A

Follow this link for commonly asked questions at NIH View it Now!

Follow this link to the NIH Office of Extramural Research page View it Now!