Clinical Research Associate (CRA) Training
Gain essential expertise as a Clinical Research Associate through this course covering ICH-GCP compliance, informed consent processes, oncology trial monitoring, protocol and IP management, source data verification, CAPA development, and inspection readiness. Perfect for clinical professionals transitioning into impactful research positions in Botswana'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 course equips you with practical skills to monitor clinical trials effectively and in full compliance. Key topics include ICH-GCP informed consent standards, vital regulatory documents, investigator site files, investigational product accountability, 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 IRB requirements to conduct compliant, inspection-ready clinical trials efficiently.
- Monitor oncology studies by verifying data accuracy, resolving queries, and ensuring patient safety.
- Manage protocols and investigational products, including deviation tracking, dosing schedules, and accountability.
- Oversee informed consent procedures with version control, re-consent protocols, and IRB notifications.
- Create CAPA plans and monitoring reports to document issues, 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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