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Clinical Trial Ethics Internships

Clinical trial ethics internships โ€” GCP / ICH compliance, informed-consent oversight, trial monitoring, and ethics-board documentation.

What is a Clinical Trial Ethics Internship?

This internship focuses on the ethical and procedural integrity of clinical trials. You see how trials are kept compliant from first protocol draft to final report โ€” and what an ethics committee actually expects to see at each step.

What you will do

  • Study GCP (E6) and ICH guideline requirements section by section
  • Audit-prep representative trial documentation โ€” protocols, ICFs, CRFs
  • Review informed-consent processes for clarity and ethical robustness
  • Shadow monitoring-visit prep and ethics committee submissions
  • Compile a compliance-checklist deliverable for an end-to-end mock trial

What you take away

  • NTHRYS internship certificate detailing trial-ethics scope
  • Operational understanding of GCP / ICH on the ground
  • Practical exposure that CRO / sponsor employers value highly
  • A profile fit for clinical research coordination, monitoring, and quality roles

Pick the field below to see specific clinical trial ethics project options.

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