CCRC CCRC - Certified Clinical Research Coordinator Ethics and Compliance in Clinical Research Questions and Answers 2

Question 1

A study participant who is enrolled in a clinical trial later loses decision-making capacity. What is the ethical obligation of the research team?

Accepted Answer

Obtain consent from a legally authorized representative (LAR) to continue participation

Answer

When a participant loses capacity, ongoing research participation requires consent from a legally authorized representative unless the IRB has approved a waiver.

Question 2

Which principle from the Belmont Report most directly supports the requirement for informed consent?

Accepted Answer

Respect for Persons

Answer

Respect for Persons requires acknowledging individuals as autonomous agents capable of making their own decisions, which is operationalized through the informed consent process.

Question 3

When is a waiver of informed consent permissible for non-exempt research under the US Common Rule (45 CFR 46)?

Accepted Answer

When the research involves no more than minimal risk, cannot practicably be carried out without the waiver, and rights are not adversely affected

Answer

Under 45 CFR 46.116(f), a waiver of consent may be granted if the research poses no more than minimal risk, cannot practicably be conducted otherwise, and does not adversely affect participant rights.

Question 4

What is the ethical rationale for including women and minorities as required participants in federally funded clinical research in the US?

Accepted Answer

To satisfy NIH Revitalization Act requirements ensuring results are generalizable across populations

Answer

The NIH Revitalization Act of 1993 mandates inclusion of women and minorities in federally funded research so that findings are applicable to all segments of the US population.

Question 5

A coordinator discovers that a colleague has been entering fabricated lab values into the study database. What is the appropriate response?

Accepted Answer

Report the concern to the PI, IRB, and institutional research integrity office

Answer

Data fabrication is research misconduct; the coordinator has an ethical and regulatory obligation to report it to the PI, IRB, and the institution's research integrity office.

CCRC - Certified Clinical Research Coordinator Practice Test

CCRC - Certified Clinical Research Coordinator Practice Test

CCRC CCRC - Certified Clinical Research Coordinator Ethics and Compliance in Clinical Research Questions and Answers 2