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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 full compliance. Key topics include ICH-GCP informed consent standards, vital regulatory files, site file organization, investigational product tracking, handling protocol deviations, source data verification and eCRF methods, serious adverse event management, corrective action plans, monitoring visit processes, and preparing for inspections in oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP guidelines and IRB processes to conduct compliant, inspection-ready clinical trials efficiently.
  • Monitor oncology studies by validating data accuracy, resolving queries, and ensuring patient safety.
  • Manage protocols and investigational products by tracking deviations, dosing schedules, and drug accountability.
  • Oversee informed consent with proper version controls, re-consent protocols, and IRB notifications.
  • Create CAPA plans and monitoring reports to record observations, identify trends, and improve 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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