Clinical Research Associate (CRA) Training
Gain essential expertise as a Clinical Research Associate through this course on informed consent processes, ICH-GCP standards, oncology trial protocols, source data verification techniques, corrective and preventive actions, and readiness for regulatory inspections. Perfect for healthcare workers transitioning into vital clinical research positions in Namibia and beyond.

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 key skills to monitor clinical trials effectively and in full compliance. Covering ICH-GCP informed consent, vital regulatory files, site file organisation, investigational product tracking, protocol deviations, source data verification and eCRF methods, serious adverse event management, corrective action plans, monitoring processes, and preparation for inspections in oncology and other studies.
Elevify advantages
Develop skills
- Master ICH-GCP and ethics committee basics to conduct compliant, inspection-ready trials efficiently.
- Oversee oncology studies by checking data accuracy, handling queries, and ensuring patient wellbeing.
- Manage protocols and study drugs by monitoring deviations, dosing times, and accountability.
- Guide informed consent procedures with version tracking, re-consent protocols, and ethics reporting.
- Create corrective action plans and reports to record observations, 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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