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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 course develops practical abilities to monitor clinical trials effectively and in full compliance. Participants gain knowledge in ICH-GCP informed consent standards, key regulatory files, investigator site organisation, investigational product tracking, protocol noncompliance, source data verification and electronic case report form methods, serious adverse event management, corrective action plans, monitoring procedures, and preparation for audits across oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and ethics committee requirements to conduct compliant and audit-ready trials efficiently.
  • Oversee oncology clinical trials by validating data, resolving queries, and ensuring participant safety.
  • Manage protocols and investigational products through deviation monitoring, dosing schedules, and accountability.
  • Direct informed consent procedures including version management, re-consent protocols, and ethics reporting.
  • Develop corrective action plans and reports to record observations, identify patterns, 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

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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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