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 effective site communications using tailored tools, checklists, and templates for Phase II hospital trials. This course equips you with hands-on expertise to ensure data integrity, minimise deviations, and prepare for inspections in asthma studies.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
This Clinical Trial Assistant (CTA) Course delivers practical, step-by-step training for supporting compliant Phase II asthma studies. Master GCP fundamentals, protocol compliance, adverse event identification, and precise source-to-eCRF reconciliation. Access ready-to-implement CAPA frameworks, consent validation tools, logs, trackers, and communication templates to boost data accuracy, cut down deviations, and maintain inspection readiness.
Elevify advantages
Develop skills
- Master AE reporting: swiftly identify, record, and report safety issues.
- Achieve GCP and regulatory expertise: implement ICH guidelines, ethics, and AE protocols in routine trial tasks.
- Control informed consent: handle ICF updates, re-consenting, and maintain audit-compliant records.
- Develop root cause analysis and CAPA expertise: investigate deviations and create robust corrective plans.
- Excel in CTA operations: assist with monitoring visits, eCRF verification, and 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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