Clinical Trial Assistant (CTA) Course
Acquire practical CTA skills for clinical trials in medicine: master GCP principles, AE reporting, informed consent management, protocol compliance, CAPA development, and site communications using tailored tools, checklists, and templates for Phase II hospital trials. This course equips you to enhance data integrity, minimise deviations, and prepare for inspections effectively.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
The Clinical Trial Assistant (CTA) Course delivers hands-on, step-by-step skills to assist compliant Phase II asthma studies. Master key GCP concepts, protocol compliance, adverse event identification, and precise source-to-eCRF mapping. Access practical CAPA frameworks, consent checking tools, logs, trackers, and communication templates to boost data accuracy, cut down deviations, and remain ready for audits.
Elevify advantages
Develop skills
- Gain mastery in AE reporting: swiftly spot, record, and report safety issues.
- Achieve fluency in GCP and regulations: implement ICH guidelines, ethics, and AE norms in routine tasks.
- Master informed consent processes: handle ICF updates, re-consent procedures, and maintain audit-ready records.
- Develop root cause analysis and CAPA expertise: investigate deviations and create strong corrective plans.
- Excel in CTA operations: aid monitoring visits, verify eCRF data, 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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