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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. Covering ICH-GCP standards, you'll master informed consent processes, key regulatory documents, site file organisation, investigational product accountability, handling protocol deviations, source data verification and eCRF practices, serious adverse event management, corrective action plans, monitoring visit procedures, and preparation for inspections across oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB requirements to conduct compliant, inspection-ready clinical trials efficiently.
  • Monitor oncology studies by verifying data accuracy, resolving queries, and ensuring patient safety.
  • Manage protocols and investigational products, including deviation tracking, dosing schedules, and accountability.
  • Oversee informed consent processes with version control, re-consenting procedures, and IRB notifications.
  • Develop CAPA plans and monitoring reports to record findings, identify trends, 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 I work for.
SilviaNurse
Great course. A lot of valuable information.
WiltonCivil Firefighter

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