​Bill of Rights and Responsibilities for HIV Research 

The cross-network Bill of Rights and Responsibilities for HIV Research document provides a short list of the rights and responsibilities for participants in a clinical trial. The purpose of this document is to help research participants act on their own behalf and in partnership with study staff. Rights and responsibilities listed in the document are in no particular rank order. This document was developed by the Community Partners Bill of Rights and Responsibilities Working Group for use by sites, at their discretion, along with informed consent forms. Feel free to share this resource with collaborators both within and outside the HIV/AIDS Clinical Trials Networks.  

View the Document​​​

​Recommendations for Community Involvement in NIAID Clinical Trials Networks

The National Institute of Allergy and Infectious Diseases (NIAID), Division of AIDS (DAIDS) and Community Partners have provided a tool for researchers and community representatives to further expand and deepen existing partnerships and forge new ones in clinical trials research. Now also available in Portuguese.

View the Documents​

TB Res​ources for Communities

Community Partners and the TB Community Research Advisors Group (CRAG) partnered to help educate community members and researchers about HIV, TB, and how the two diseases are connected. Find links to quick facts, videos, and much more.​

More information​​

Webinars & ​Training 

​​Community Partners Webinars

Community Partners hosts a number of webinars throughout the year focused on topics relevant to community and HIV research.​ More information​​

​​CAB Training

The Community Partners Training Working Group (CTWG) created a set of standardized, high quality CAB training materials for cross-network use. More information

​​BTG Training Modules

Be the Generation developed two training modules for community staff. Click below to learn more:

• Basic Scientific Literacy (BSL) Training

• HIV Prevention Research (HPR) Training​