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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?

This focused Clinical Research Associate (CRA) Training course develops practical abilities to monitor clinical trials effectively and in full compliance. Participants will cover ICH-GCP informed consent standards, key regulatory documents, investigator site file organisation, investigational product accountability, protocol deviations, source data verification and electronic case report form practices, serious adverse event management, corrective and preventive action development, monitoring visit procedures, and preparation for inspections across oncology and non-oncology studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB essentials to conduct compliant, inspection-ready trials efficiently.
  • Monitor oncology trials by verifying data, managing queries, and safeguarding patient safety.
  • Manage protocols and investigational products by tracking deviations, dosing windows, and drug accountability.
  • Oversee informed consent processes including version control, re-consent procedures, and IRB reporting.
  • Develop CAPA plans and reports to document findings, identify trends, and enhance 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

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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. Lots of valuable information.
WiltonCivil Firefighter

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