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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?

Dis concise CRA Training course build practical skills fi monitor trials confident an compliant. Yuh wi learn ICH-GCP align informed consent, key regulatory docs, investigator site file setup, IP accountability, protocol deviations, SDV an eCRF best practices, SAE handling, CAPA design, monitoring visit flows, an inspection readiness fi top-quality oncology an non-oncology studies.

Elevify advantages

Develop skills

  • Master ICH-GCP an IRB essentials: run compliant, inspection-ready trials quick-quick.
  • Monitor oncology trials: check data, handle queries, an protect patient safety proper.
  • Control protocol an IP: track deviations, dosing windows, an drug accountability tight.
  • Lead informed consent: use version control, re-consent steps, an IRB reporting right.
  • Design CAPA an reports: document findings, spot trends, an boost site quality strong.

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 are saying

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EmersonPolice Investigator
The course was essential to meet my boss's and the company's expectations.
SilviaNurse
Really great course. Lots of valuable information.
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