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Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training
from 4 to 360h flexible workload
certificate valid 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 organisation, investigational product tracking, handling protocol deviations, source data verification and eCRF practices, 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 and ethics board requirements to conduct compliant, inspection-ready clinical trials swiftly.
  • Monitor oncology studies by validating data, resolving queries, and safeguarding participant wellbeing.
  • Manage protocols and investigational products by logging deviations, dosing schedules, and accountability.
  • Oversee informed consent procedures with version tracking, 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 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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