Clinical Trial Researcher

A Clinical Trial Researcher is a researcher that is involved in a clinical trial is responsible for ensuring that clinical trial protocols and applicable regulations are followed.

• AKA: Clinical Investigator.
• Example(s):
  • a Clinical Study Coordinator,
  • a clinician who is responsible for clinical trial,
  • a healthcare provider who is responsible for clinical trial,
  • …
• Counter-Example(s):
  • Clinician,
  • Healthcare Provider.
• See: European Medicines Agency, Clinical Trial, Food And Drug Administration.

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References

2021a

• (Wikipedia, 2021) ⇒ https://en.wikipedia.org/wiki/Clinical_investigator Retrieved:2021-11-21.
  • A clinical investigator involved in a clinical trial is responsible for ensuring that an investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations; for protecting the rights, safety, and welfare of subjects under the investigator's care; and for the control of drugs under investigation. The Clinical Investigator must also meet requirements set forth by the FDA, EMA or other regulatory body. The qualifications must be outlined in a current resume and readily available for auditors.

2021b

• (Wikipedia, 2021) ⇒ https://en.wikipedia.org/wiki/Glossary_of_clinical_research Retrieved:2021-11-21.
  • Clinical investigator
    • A medical researcher in charge of carrying out a clinical trial's protocol. (NLM)
  • (...)
  • Clinical researcher
    • A health professional who works directly with patients, or uses data from patients, to do research on health and disease and to develop new treatments. Clinical researchers may also do research on how health care practices affect health and disease. (NCI)

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