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Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training
flexible workload from 4 to 360h
valid certificate in your country

What will I learn?

This concise Clinical Research Associate (CRA) Training course builds practical skills to monitor trials confidently and compliantly. You will learn ICH-GCP–aligned informed consent requirements, essential regulatory documents, investigator site file structure, IP accountability, protocol deviations, SDV and eCRF best practices, SAE handling, CAPA design, monitoring visit workflows, and inspection readiness for high-quality oncology and non-oncology studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB essentials: run compliant, inspection-ready trials fast.
  • Monitor oncology trials: verify data, manage queries, and protect patient safety.
  • Control protocol and IP: track deviations, dosing windows, and drug accountability.
  • Lead informed consent: apply version control, re-consent steps, and IRB reporting.
  • Design CAPA and reports: document findings, trend issues, and drive site quality.

Suggested summary

Before starting, you can change the chapters and workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.
Workload: between 4 and 360 hours

What our students say

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Very great course. Lots of valuable information.
WiltonCivil Firefighter

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