Clinical Research Associate (CRA) Training
Gain essential Clinical Research Associate skills like ICH-GCP compliance, informed consent processes, oncology trial monitoring, protocol and IP control, source data verification, CAPA development, and inspection readiness. Perfect for clinical workers entering impactful research positions in Nigeria's growing health sector.

from 4 to 360h flexible workload
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 verification and eCRF methods, serious adverse event management, CAPA creation, monitoring processes, and inspection preparation for oncology and other studies.
Elevify advantages
Develop skills
- Master ICH-GCP and IRB basics to manage compliant, inspection-ready trials quickly.
- Monitor oncology studies by checking data, handling queries, and ensuring patient safety.
- Manage protocols and drug supply with deviation tracking, dosing schedules, and accountability.
- Handle informed consent using version controls, re-consent procedures, and IRB updates.
- Create CAPA plans and reports to record findings, spot trends, and improve 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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