The event is supported by Fogarty, International Development Research Centre (IDRC), UK Medical Research Council (MRC), and Wellcome Trust, and will serve as a pilot to help determine if there is sufficient interest in a recurring event in the future.
The event will bring researchers and humanitarian organizations together to share experiences and promote collaboration around health research in humanitarian settings, modelled after the Global Forum on Bioethics in Research (which Fogarty also supports). The target audience is early- to mid-career researchers from LMICs and countries affected by humanitarian crises, though the applications are open to all interested parties.
Applications are invited for case study presenters and general participants, with a submission deadline of May 28, 2021.
The following themes for case studies for the upcoming Global Forum on Humanitarian Health Research may be of interest (announcement below). Case studies to be presented at GFH2R should relate specifically to the theme of “Research in the Context of Concurrent Crises.” Questions that could be explored in the case studies include, but are not limited to:
• What are the key ethical considerations for researchers working in the context of multiple humanitarian crises? What are some specific ethical dilemmas in these settings?
• How can researchers better engage with communities living in humanitarian crises?
• How can research provide an opportunity for inclusion and nurture leadership of local actors in problem solving in such contexts?
• What are specific experiences and good practices related to the study of specific subpopulations (e.g. vulnerable populations, women, children, etc.)?For more information visit https://www.fic.nih.gov/About/center-global-health-studies/Pages/health-research-humanitarian-crises-global-forum.aspx
The Stop
TB Partnership Working Group on New TB Vaccines (WGNV) and the National
Institute for Allergy and Infectious Diseases (NIAID)are
co-hosting a workshop on the topic of Recognition and Control of Mtb
Infected Cells: From Basics to the Clinic. This workshop is intended to address
the need for correlates and to identify platforms that measure recognition or
control of the infected cell - especially in humans - as identified in the EDCTP/AIGHD Global Roadmap for
Research and Development of New TB Vaccines and the Strategic Framework for
New TB Vaccines in the Stop TB Partnership Global Plan to End TB 2023 - 2030.
The overall goals of this workshop
are to:
The workshop format will be largely
discussion-based. Each session will have three short presentations that will
provide a high-level overview of key topics within the session theme, followed
by a discussion between the session chairs, speakers, and participants.
Click here
to view the programme and
speakers.
This workshop is free of charge and
open to any participants interested in this topic.
The International Society for Infectious Diseases (ISID) and the Swiss
Society for Infectious Diseases (SSI) are inviting applications for their joint
Infectious Diseases Research Fellowship Program. The purpose of this programme
is to support infectious disease physicians and scientists from under-resourced
countries through multidisciplinary clinical and laboratory training at a
select biomedical institution in Zurich, Switzerland. The one-year SSI/ISID
Fellowship programme is open to applicants who are 40 years or younger,
citizens and permanent residents of under-resourced countries or Eastern
Europe. The deadline for applications is 16 June 2023.
More information: https://na.eventscloud.com/eSites/748378/Homepage
The MRCT Center and Medable convened a multi-stakeholder task force to address ethical and regulatory opportunities and challenges related to Decentralized Clinical Trials (DCTs). Join them on June 20, from 10 - 11 AM ET, for a joint webinar entitled, "Ethical Review of Decentralized Clinical Trials (DCTs): Tools, Resources & Best Practices."
During the webinar, Barbara Bierer (MRCT Center), Pam Tenaerts
(Medable) and Leanne Madre (Medable) will present a framework, recommendations,
and tools organized around 3 DCT domains: People, Remote Data Collection, and
Data Oversight. Best practices for the ethical review, approval, and conduct of
DCTs will be provided.
Clinical trial stakeholders (IRB/ECs,
HRPP, sites, sponsors, investigators, and others) to register for the webinar here