Clinical Research Associate Course
This course equips aspiring Clinical Research Associates with essential skills for effective trial monitoring, regulatory compliance, and documentation management.

flexible workload of 4 to 360h
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. You will learn to design CAPA, review informed consent, perform SDV and ensure data integrity, check eligibility, detect and report SAEs, and manage IMP accountability. Develop skills for inspection-ready documentation using clear templates, SOP-based processes, and targeted monitoring strategies right from the start.
Elevify advantages
Develop skills
- SAE safety oversight: detect, document, and escalate serious events quickly.
- IMP 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 workloadWhat our students say
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