Clinical Research Associate Course
This course equips aspiring Clinical Research Associates with essential skills for monitoring clinical trials effectively and compliantly, covering key areas like adverse event management, product accountability, eligibility checks, CAPA processes, and informed consent verification to ensure inspection-ready practices from day one.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
The Clinical Research Associate Course provides practical, step-by-step training to monitor trials confidently and in compliance with regulations. Learn CAPA design, informed consent review, source data verification and data integrity, eligibility checks, serious adverse event detection and reporting, and investigational medicinal product accountability. Develop skills for inspection-ready documentation and apply clear templates, standard operating procedure-based processes, and targeted monitoring strategies right from the start.
Elevify advantages
Develop skills
- Serious adverse event safety oversight: detect, document, and escalate serious events quickly.
- Investigational medicinal product accountability: reconcile drug logs, returns, storage, and temperature conditions.
- Eligibility verification: confirm criteria and resolve source data conflicts.
- CAPA execution: design, document, and track corrective and preventive actions.
- Informed consent review: verify timing, signatures, and complete documentation.
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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