Investigator Responsibilities

Bruce J. Giantonio ()
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Bruce J. Giantonio: The ECOG-ACRIN Cancer Research Group

Chapter 6 in Principles and Practice of Clinical Trials, 2022, pp 85-95 from Springer

Abstract: Abstract The research atrocities committed during World War II using human subjects prompted the development of a body of regulations, beginning with the Nuremberg Code, to ensure that human subjects’ research is safely conducted and prioritizes the rights of the individual over the conduct of the research. The resultant regulations guiding human subjects’ research affect protocol design, the selection of participants, safety reporting and oversight, and the dissemination of research results. The investigator conducting research on human subjects must be familiar with those regulations to meet his/her responsibility to protect the rights and welfare of research participants.

Keywords: Belmont Report; The Common Rule; Delegation of tasks; Drug accountability; Good clinical practice; Informed consent process; Institutional review board (IRB); Investigator; Noncompliance; Scientific misconduct (search for similar items in EconPapers)
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:spr:sprchp:978-3-319-52636-2_29

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DOI: 10.1007/978-3-319-52636-2_29

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