Large volumes of health-related data are collected from various sources we use every day, including computers, smartphones, tablets, and wearable devices. Anonymised health data are also collected by medical insurance companies in the private health sector and official public health databases to design treatment and prevention strategies to address various public health issues and benefit communities. However, there is a lack of awareness among the public that this data is being collected and shared. When this data is collected from an individual it is very personal and sensitive, but once anonymised as part of large data sets, it cannot easily be linked back to the individual. How should we engage with communities, using simple non-technical language, to raise awareness that sensitive individual health and location information is being collected and shared as part of a large, anonymised data set? Research for Ethical Data Science in sub-Saharan Africa (REDSSA) is seeking ideas for strategies to help improve transparency, understanding and trust in large data-driven health research for the public good. Deadline for submission: 30 April 2023.
More information https://www.sun.ac.za/english/faculty/healthsciences/cmel/redssa/crowdsourcing
Read moreOn Thursday 30 March, the Working Group on New TB Vaccines Early Career Researcher Network is organizing a virtual discussion session. Dr. Alan Sher (NIAID/NIH) will talk about how to start up and maintain a successful research group, including managing the complex diversity of trainees while balancing the requirements and expectations of being a group leader. The session will take place at 6am PDT / 9am EDT / 3pm CEST and SAST / 6:30pm IST.
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