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Clinical Research Associate (CRA) Training

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

What will I learn?

This focused CRA Training course equips you with hands-on skills to monitor clinical trials effectively and in full compliance. You'll cover ICH-GCP informed consent standards, key regulatory files, site file organisation, investigational product tracking, handling protocol deviations, source data verification and eCRF practices, serious adverse event management, corrective action plans, monitoring visit processes, and preparing for inspections in oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB basics to conduct compliant, inspection-ready trials swiftly.
  • Monitor oncology studies by checking data, resolving queries, and ensuring patient safety.
  • Manage protocols and drugs by logging deviations, dosing times, and accountability.
  • Oversee informed consent with version tracking, re-consent procedures, and IRB updates.
  • Create CAPA plans and reports to record issues, spot patterns, and improve site performance.

Suggested summary

Before starting, you can change the chapters and the 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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