Clinical Trial Assistant (CTA) Course
Gain practical CTA expertise for clinical trials: master GCP compliance, adverse event reporting, informed consent management, protocol adherence, CAPA development, and site coordination using tailored tools, checklists, and templates for Phase II hospital trials.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Clinical Trial Assistant (CTA) Training equips you with hands-on skills to support compliant asthma Phase II clinical studies. Master GCP principles, protocol compliance, adverse event identification, and precise source-to-eCRF reconciliation. Access practical CAPA frameworks, consent verification aids, logs, trackers, and communication templates to boost data integrity, minimise deviations, and ensure inspection readiness.
Elevify advantages
Develop skills
- Master adverse event reporting: swiftly identify, record, and report safety incidents.
- Achieve GCP and regulatory proficiency: implement ICH guidelines, ethics, and safety protocols daily.
- Control informed consent processes: handle ICF updates, re-consent, and maintain audit-ready records.
- Develop root cause analysis and CAPA expertise: investigate deviations and create robust corrective plans.
- Excel in CTA operations: assist monitoring visits, verify eCRF data, and enforce protocol compliance.
Suggested summary
Before starting, you can change the chapters and 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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