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Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training
4 to 360 hours flexible workload
valid certificate in your country

What will I learn?

Gain practical skills for confident, compliant trial monitoring in this CRA training. Learn ICH-GCP informed consent, key regulatory documents, site file setup, IP tracking, protocol deviations, SDV and eCRF practices, SAE management, CAPA creation, visit workflows, and inspection prep for oncology and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB essentials to run compliant, inspection-ready trials.
  • Monitor oncology trials by verifying data, managing queries, and ensuring patient safety.
  • Control protocols and IP through tracking deviations, dosing windows, and drug accountability.
  • Lead informed consent processes with version control, re-consent steps, and IRB reporting.
  • Design CAPA and reports to document findings, trend issues, and improve site quality.

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

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 I work for.
SilviaNurse
Really great course. Lots of valuable information.
WiltonCivil Firefighter

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