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Clinical Research Associate (CRA) Training

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

What Will I Learn?

This focused Clinical Research Associate (CRA) Training course equips you with practical skills to monitor clinical trials effectively and in compliance. Key topics include ICH-GCP informed consent, regulatory documents, site file organisation, investigational product accountability, protocol deviations, source data verification, eCRF practices, serious adverse event management, corrective action plans, monitoring workflows, and inspection readiness for oncology and other studies.

Elevify Advantages

Develop Skills

  • Master ICH-GCP and IRB requirements to conduct compliant, inspection-ready trials efficiently.
  • Monitor oncology trials by verifying data accuracy, resolving queries, and ensuring patient safety.
  • Manage protocols and investigational products, tracking deviations, dosing, and accountability.
  • Oversee informed consent with version control, re-consent procedures, and IRB notifications.
  • Develop CAPA plans and reports to document issues, identify trends, and enhance 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

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

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