The organization and responsibilities of the health care professions have changed as a result of changes in how new pharmaceuticals are generated, particularly the privatization of clinical trials. We look at one facet of this change: the function of research coordinators in American contract research.
Our attention to coordinators draws attention to the moral dilemmas present in clinical trials. We outline how coordinators deal with the tension between research and care and demonstrate how their idea of ethics differs from institutional conceptions traditionally connected with human subjects' research. Our analysis shows how the coordinators' emphasis on ethics is a reaction to their role conflict and an effort to reintroduce personalized care into the environment of research.
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