Abstract
In the wake of Europe’s General Data Protection Regulation (GDPR), research ethics governance does not just affect the ethical dimensions of social research but also the range of scientific decisions available to researchers. Because of the sensitive status of personal data and the aversion to even minimal risk by what we call “moral bureaucracies”, we are concerned that social network researchers will increasingly limit their research decisions to “safe” options, like reusing anonymized datasets, choosing target populations based on convenience rather than theoretical relevance, and routinely subcontracting fieldwork to professional data collection companies, among others. We also suggest that scientific associations and social scientists in general need to adopt a proactive role in preserving both scientific freedom and genuine ethics advice within this new regulatory framework.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
