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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 Clinical Research Associate (CRA) Training course develops practical abilities to monitor clinical trials effectively and in line with regulations. Learners gain knowledge in ICH-GCP compliant informed consent, key regulatory files, site file organisation, investigational product tracking, protocol deviation management, source data verification and eCRF practices, serious adverse event processes, corrective action plans, monitoring procedures, and readiness for audits in oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP guidelines and IRB procedures to conduct compliant and audit-ready clinical trials efficiently.
  • Oversee oncology clinical trials by validating data accuracy, resolving queries, and ensuring participant safety.
  • Manage protocol adherence and investigational products through deviation tracking, dosing schedules, and accountability measures.
  • Handle informed consent effectively with version management, re-consent protocols, and IRB notifications.
  • Create corrective action plans and monitoring 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 I work for.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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