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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 focused Clinical Research Associate (CRA) Training builds key skills for confident and compliant trial monitoring. Learners cover ICH-GCP informed consent rules, vital regulatory files, site file setup, drug accountability, protocol issues, source data checks and eCRF methods, serious adverse event management, corrective action plans, monitoring processes, and readiness for audits in cancer and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and ethics board basics to manage compliant, audit-ready trials quickly.
  • Oversee cancer trials by checking data, handling queries, and ensuring patient safety.
  • Manage study protocols and drug supplies, including deviations, dosing times, and accountability.
  • Guide informed consent with version tracking, re-consent procedures, and ethics reporting.
  • Create corrective plans and reports to record issues, spot patterns, and improve site standards.

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

I was just promoted to Intelligence Advisor for the Prison System, and the course from Elevify was crucial for me to be selected.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of valuable information.
WiltonCivil Firefighter

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