Clinical Trial Assistant (CTA) Course
Acquire essential CTA competencies for clinical trials in Phase II asthma studies: gain expertise in GCP principles, adverse event management, informed consent processes, protocol compliance, CAPA development, and site communications using practical checklists, templates, and tools for superior data integrity and regulatory preparedness.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
This Clinical Trial Assistant (CTA) Course equips you with hands-on, sequential skills for supporting compliant Phase II asthma clinical studies. Master key GCP principles, protocol compliance, adverse event identification, and precise source data to eCRF reconciliation. Access practical CAPA frameworks, consent validation aids, tracking logs, and communication templates to boost data accuracy, minimise deviations, and ensure inspection readiness.
Elevify Advantages
Develop Skills
- Master adverse event reporting by swiftly identifying, recording, and escalating safety issues.
- Achieve proficiency in GCP and regulations by implementing ICH guidelines, ethics, and AE protocols in routine trial tasks.
- Handle informed consent effectively, including ICF version control, re-consenting, and maintaining audit-compliant records.
- Develop root cause analysis and CAPA expertise to investigate deviations and create robust corrective plans.
- Excel in CTA operations by aiding monitoring visits, verifying eCRF data, and ensuring 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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