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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 equips you with hands-on skills to monitor clinical trials effectively and in line with regulations. 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 preparation for inspections in oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and ethics committee requirements to conduct compliant, inspection-ready trials efficiently.
  • Monitor oncology studies by validating data, resolving queries, and ensuring patient safety.
  • Manage protocols and investigational products, including deviation tracking, dosing schedules, and accountability.
  • Oversee informed consent with version management, re-consent procedures, and ethics reporting.
  • Develop corrective actions and reports to record findings, identify 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 my boss's and the company's expectations.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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