Clinical Trial Assistant (CTA) Course
Gain practical CTA expertise for clinical trials: excel in 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 in asthma studies.

flexible workload from 4 to 360h
valid certificate in your country
What will I learn?
This Clinical Trial Assistant (CTA) Course equips you with hands-on, step-by-step abilities to assist in compliant asthma Phase II clinical studies. Master key GCP principles, protocol compliance, adverse event spotting, and precise source data to eCRF matching. Acquire practical CAPA strategies, consent checking tools, logs, trackers, and communication aids to boost data accuracy, minimise errors, and prepare for audits.
Elevify advantages
Develop skills
- Master adverse event reporting: spot, record, and report safety issues swiftly.
- Achieve GCP and regulatory proficiency: implement ICH guidelines, ethics, and safety protocols daily.
- Control informed consent: handle ICF updates, re-consenting, and maintain audit-proof 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 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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