Developing a Successful Grant Application

Allowable Costs for Clinical Research Participation

When thinking about participant recruitment in NIH supported clinical studies, researchers should ensure they are planning for the recruitment and retention of people across the life span, women, and racial and ethnic minorities, as appropriate, as well as considering which costs may be allowable throughout the project for their participation. In this episode of the NIH All About Grants podcast, Dr.

Considering Language Access for Participants in NIH-Supported Clinical Research

This episode of the NIH All About Grants podcast explores language access for participants in NIH supported clinical research. Ms. Melissa McGowan, the Deputy Director of the Office of Clinical Research within the National Institute on Aging’s Division of Extramural Activities, and Ms. Dawn Corbett, NIH’s Inclusion Policy Officer, will explain how to consider language access when proposing research in a grant application.

Ins and Outs of Training Grants (miniseries) Part 1

Institutional training grants help prepare undergraduates, predoctoral students and postdoctoral scholars for careers in biomedical and behavioral research. Part 1 of this NIH All About Grants podcast miniseries dives into considerations for developing training grant applications and the review process, and part 2 focuses on post-award monitoring, mentorship, and provides insights for trainees.

Responsible Conduct of Research and Training

A fundamental part of one’s growth as a researcher is understanding how scientific investigation is practiced with integrity, and knowing when and how to apply professional norms and ethical principles throughout the research process. To promote research integrity, NIH-supported trainees, fellows, participants, and scholars must receive instruction in the responsible conduct of research (RCR).

Phase III Trials

NIH’s definition of a Phase III clinical trial is quite broad, including drug studies, device studies, behavioral interventions, epidemiological studies, community trials, and more. Phase III trials are usually large, prospective trails that compare two or more interventions against other standard or experimental interventions.

Sex As a Biological Variable

NIH expects that sex as a biological variable (SABV) will be factored into research designs, analyses, and reporting in pre-clinical and clinical studies. Accounting for SABV helps interpret and validate research findings, as well as enhances the rigor, reproducibility, and applicability of biomedical research. But how exactly do you account for SABV?

Building Bridges

You may have heard that NIH can provide limited, interim research support for applications with creative and innovative approaches that fell just outside the payline. These “bridge awards” are helpful for researchers to gather additional data to revise their current application. But, how do we decide on which applications to support this way?


This page last updated on: November 21, 2024
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