Clinical Research Associate (CRA) Training
Gain essential expertise as a Clinical Research Associate through this course covering informed consent processes, ICH-GCP guidelines, oncology trial protocols, source data verification, corrective and preventive actions, and inspection preparedness. Perfect for clinical workers transitioning to vital research monitoring positions in diverse therapeutic areas.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This focused Clinical Research Associate (CRA) Training course equips you with hands-on skills to monitor clinical trials effectively and in full compliance. Key topics include ICH-GCP informed consent standards, vital regulatory files, site file organisation, investigational product tracking, handling protocol deviations, source data verification and eCRF practices, serious adverse event management, corrective action plans, monitoring visit processes, and preparing for inspections in oncology and other studies.
Elevify advantages
Develop skills
- Master ICH-GCP and ethics board requirements to conduct compliant, inspection-ready trials efficiently.
- Monitor oncology studies by validating data, resolving queries, and ensuring patient safety.
- Manage protocols and investigational products, including deviation tracking, dosing schedules, and accountability.
- Oversee informed consent with version controls, re-consent procedures, and ethics reporting.
- Develop corrective action plans and reports to record findings, identify trends, and improve site performance.
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.What our students say
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