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Clinical Research Associate (CRA) Training

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

What will I learn?

Gain practical skills for confident, compliant trial monitoring in this CRA training. Cover ICH-GCP informed consent, key regulatory documents, site file organization, IP accountability, protocol deviations, SDV and eCRF practices, SAE management, CAPA creation, monitoring workflows, and inspection preparation for oncology and non-oncology trials.

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 by 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 Correctional 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
Great course. Lots of valuable information.
WiltonCivil Firefighter

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