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 techniques, corrective and preventive actions, and inspection preparedness. Perfect for healthcare workers transitioning into demanding clinical research positions in Zambia or beyond, ensuring trials meet global standards safely and efficiently.

from 4 to 360h flexible workload
certificate valid 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 clinical trials swiftly.
- Monitor oncology studies by validating data, resolving queries, and safeguarding participant wellbeing.
- Manage protocols and investigational products by logging deviations, dosing schedules, and accountability.
- Oversee informed consent procedures with version tracking, re-consent protocols, and ethics reporting.
- Develop corrective action plans and reports to record observations, identify patterns, and enhance site performance.
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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