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Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training
from 4 to 360h flexible workload
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 verification and eCRF methods, serious adverse event management, CAPA creation, monitoring processes, and inspection preparation for oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB basics to manage compliant, inspection-ready trials quickly.
  • Monitor oncology studies by checking data, handling queries, and ensuring patient safety.
  • Manage protocols and drug supply with deviation tracking, dosing schedules, and accountability.
  • Handle informed consent using version controls, re-consent procedures, and IRB updates.
  • Create CAPA plans and reports to record findings, spot trends, and improve site performance.

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 where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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