Clinical Research Associate (CRA) Training
Gain essential Clinical Research Associate skills like informed consent processes, ICH-GCP standards, oncology study protocols, source data verification, corrective actions, and audit preparation. Perfect for health workers stepping into vital clinical trial positions in demanding research environments.

flexible workload from 4 to 360h
valid certificate in your country
What will I learn?
This focused Clinical Research Associate (CRA) Training builds key skills for confident and compliant trial monitoring. Learners cover ICH-GCP informed consent rules, vital regulatory files, site file setup, drug accountability, protocol issues, source data checks and eCRF methods, serious adverse event management, corrective action plans, monitoring processes, and readiness for audits in cancer and other studies.
Elevify advantages
Develop skills
- Master ICH-GCP and ethics board basics to manage compliant, audit-ready trials quickly.
- Oversee cancer trials by checking data, handling queries, and ensuring patient safety.
- Manage study protocols and drug supplies, including deviations, dosing times, and accountability.
- Guide informed consent with version tracking, re-consent procedures, and ethics reporting.
- Create corrective plans and reports to record issues, spot patterns, and improve site standards.
Suggested summary
Before starting, you can change the chapters and workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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