Clinical Trial Assistant (CTA) Course
Acquire practical CTA skills for clinical trials: master GCP principles, adverse event reporting, informed consent management, protocol compliance, CAPA development, and site communications using tailored tools, checklists, and templates for Phase II asthma studies in hospital settings.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
This Clinical Trial Assistant (CTA) Course delivers hands-on skills for supporting compliant Phase II asthma trials. Master GCP fundamentals, protocol compliance, adverse event identification, and precise source-to-eCRF reconciliation. Access practical CAPA frameworks, consent verification aids, logs, trackers, and communication templates to enhance data integrity, minimise deviations, and maintain inspection readiness.
Elevify advantages
Develop skills
- Master adverse event reporting: detect, document, and escalate safety issues swiftly.
- Gain fluency in GCP and regulations: apply ICH guidelines, ethics, and AE protocols daily.
- Control informed consent processes: handle ICF versions, re-consents, and audit files.
- Develop root cause analysis and CAPA expertise: investigate deviations and create action plans.
- Achieve excellence in CTA operations: assist monitoring, verify eCRFs, and ensure protocol adherence.
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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