INSTRUCTIONS FOR "RESEARCH PROPOSAL" PORTION OF APPLICATION
Applications that exceed the page limitations listed below or that do not comply
with the required CRC application format will be returned without review.
A. Introduction:
Unestablished Investigators and Investigators
Submitting Clinical Research Studies-If submitting a revised application responding
to CRC comments from the early review process,
provide a statement specifying what significant changes have been made. Include
additions, deletions, revisions and any response to criticism contained in the
reviewers' sheets. These changes must be further identified by appropriate underlining,
indenting or changing of topography within the text.
DO NOT EXCEED 15 PAGES FOR ITEMS B-E. THE
FONT CAN NOT BE LESS THAN 11 POINT. THE 15-PAGE LIMIT AND FONT REQUIREMENTS
WILL BE STRICTLY ENFORCED. APPLICATIONS NOT MEETING THIS PAGE LIMITATION WILL
BE RETURNED.
Organize items B-E (Research Plan) to answer the questions:
- What do you intend to do
- Why is the work important?
- What has already been done?
- How are you going to do the work?
B. Specific Aim:
State concisely and realistically what
the research described in the application is intended to accomplish and/or what
hypothesis is to be tested. Do not exceed one (1) page.
C. Background and Significance:
Briefly sketch the background to the present
proposal; critically evaluate existing knowledge; and specifically identify the
gaps which the project is intended to fill. State concisely the importance of
the research described in the application by relating the specific aims to longer
term objectives. Do not exceed three (3) pages.
D. Preliminary Studies:
Applications may employ this section to
provide an account of the principal investigator's preliminary studies pertinent
to the application and/or any other information which will help to establish the
experience and competence of the investigator to pursue the proposed project.
Do not exceed eight (8) pages for the preliminary studies.
E. Research Design and Methods:
Discuss in detail the experimental design and the procedures
to be used to accomplish the specific aims of the work described in the application.
Describe the protocols to be used and the tentative sequence of the investigation.
Include the means by which the data will be analyzed and interpreted. Describe
new methodology and its advantage over existing methodology. Discuss the potential
difficulties and limitations of the proposed procedures and alternative approaches
to achieve the aims. Point out any procedures, situations or materials that may
be hazardous to personnel and the precautions to be exercised.
F. Literature Cited:
Mention the principal author's name when citing literature
in the text, but provide the complete references in a list at the end of the Research
Plan. Each citation must include the names of all authors, the name of the book
or journal, volume number, page numbers and year of publication. Although
no page limitation is specified for this part of the application, make every attempt
to be judicious in compiling the bibliography. It should be relevant and current.
It need not be exhaustive.
G. Collaborative Arrangements:
If the proposed project requires collaboration with other
individuals, describe the responsibility of each investigator.
H. Appendix:
Five (5) sets of the appendix material should be mailed to
the Office of the Associate Dean for Research and Faculty Affairs (ADRFA), mail
code 9616. Graphs, diagrams, tables and charts may be submitted as Appendix material.
For further information contact:
Nancy Austin in the Office of the Associate
Dean for Research and Faculty Affairs located at 801 N. Rutledge, 2nd Floor,
Room 2073 or call 545-7936. Hours are 8:00 a.m to 4:30 p.m. Monday through Friday.
Last update: September, 2006