- What responsibilities does a researcher have toward her or his study community?
- How might the socio-cultural status of a study community impact a researcher's actual responsibilities and perceptions of those responsibilities (by the researchers and their sponsors)? How might the ability of a subject to give informed consent impact or condition a researcher's responsibility to that subject?
- What are some factors that might impact or change a researcher's responsibility toward his or her study community? What responsibility does the researcher have to keep in contact with the study community after the trial?
- Does a researcher have a responsibility to provide the study community with access to the research data? If so, are there any limitations? What kind of access should the researcher provide?
Or address an email to bioethics@hsphsun2.harvard.edu