The Petrie-Flom Center for Health Law and Policy, Biotechnology, and Bioethics seeks a part-time research assistant for a project with Harvard Catalyst (Harvard Clinical and Translational Science Center) on challenges and innovation in human subjects research, addressing such issues as the regulatory and ethical aspects of research using electronic and online mediums, payment of research participants, models of community engagement and patient-centered research, and participant comprehension in informed consent. The work will initially involve 6-8 hours per week for 3 months. Applicants who have completed at least one year of a graduate program in law, health policy, or a related field are particularly encouraged to apply. Please contact Luke Gelinas, PhD, email@example.com.
Imagine this scenario: you are a researcher conducting a clinical trial on a promising treatment for a rare but serious heart condition. Unfortunately, you are struggling to locate and enroll enough eligible participants and your study is at risk of not completing. Then you discover a Facebook support group for precisely the condition you are studying. The group is open: you do not need to be invited or to suffer from the condition to become a member—anyone can join. Here are the eligible participants you have been looking for!
But what are your obligations in approaching members of this group for recruitment? Would such recruitment be ethically advisable? Under what conditions? And what ethical norms apply when approaching sick and potentially vulnerable people for recruitment over social media? How should you (and the IRB) evaluate this type of activity from an ethical perspective?