An increasing number of sponsors are using electronic submission systems - do not underestimate the time needed to use these systems to submit proposals. At your earliest opportunity you should ensure that:. Most electronic submission systems require a central sign-off, which means that when you submit your proposal it does not go directly to the proposed funder but instead is routed to your central research office for them to do the actual submission after they have made appropriate governance checks. You will need to leave additional time for this step.
Steps for a PI to Submit a Proposal | Research | USC
The aim of your research proposal by USC. A research proposal is a brief, well organized summing up of the research project that you propose to undertake. It lays out the central topic that your research project is based upon. It gives a rough or detailed idea to the reader about the general scope of your field of study. A reference or citations is also made to any recent deliberations on the issue in the research proposal. The knowledge on the topic in question, as it stands to date, is also discussed. In short, a research proposal also identifies the novelty of your proposed research idea.
The goal of a research proposal is twofold: to present and justify the need to study a research problem and to present the practical ways in which the proposed study should be conducted. The design elements and procedures for conducting research are governed by standards of the predominant discipline in which the problem resides, therefore, the guidelines for research proposals are more exacting and less formal than a general project proposal. Research proposals contain extensive literature reviews. They must provide persuasive evidence that a need exists for the proposed study.
The following is a compilation of answers to questions asked of FDA regarding the protection of human subjects of research. For ease of reference, the numbers assigned to the questions are consecutive throughout this section. These questions and answers are organized as follows. Under FDA regulations, an IRB is an appropriately constituted group that has been formally designated to review and monitor biomedical research involving human subjects.