Clinical Research Associate (CRA) Training
Gain essential expertise as a Clinical Research Associate through this course covering ICH-GCP compliance, informed consent procedures, oncology trial monitoring, protocol and IP management, source data verification, CAPA development, and inspection readiness. 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 organization, investigational product tracking, handling protocol deviations, source data verification and eCRF methods, 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 guidelines and IRB processes to conduct compliant, inspection-ready clinical trials efficiently.
- Monitor oncology studies by validating data accuracy, resolving queries, and ensuring patient safety.
- Manage protocols and investigational products by tracking deviations, dosing schedules, and drug accountability.
- Oversee informed consent with proper version controls, re-consent protocols, and IRB notifications.
- Create CAPA plans and monitoring reports to record observations, 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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