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

from 4 to 360h 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 line with regulations. Learn CAPA design, informed consent review, SDV and data integrity, eligibility checks, SAE detection and reporting, and IMP accountability. Develop skills for inspection-ready documentation and apply 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.
- 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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