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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 key skills to monitor clinical trials effectively and in full compliance. Covering ICH-GCP informed consent, vital regulatory files, site file organisation, investigational product tracking, protocol deviations, source data verification and eCRF methods, serious adverse event management, corrective action plans, monitoring processes, and preparation for inspections in oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and ethics committee basics to conduct compliant, inspection-ready trials efficiently.
  • Oversee oncology studies by checking data accuracy, handling queries, and ensuring patient wellbeing.
  • Manage protocols and study drugs by monitoring deviations, dosing times, and accountability.
  • Guide informed consent procedures with version tracking, re-consent protocols, and ethics reporting.
  • Create corrective action plans and reports to record observations, spot patterns, and improve site standards.

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

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 where I work.
SilviaNurse
Great course. Lots of valuable information.
WiltonCivil Firefighter

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