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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. Covers ICH-GCP informed consent, key regulatory documents, site file organisation, IP accountability, protocol deviations, SDV and eCRF best practices, SAE management, CAPA creation, monitoring workflows, and inspection preparation for oncology and non-oncology studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB essentials to run compliant, inspection-ready trials efficiently.
  • 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, identify trends, 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 chosen.
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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