Clinical Trial Management Course
This course equips professionals with essential skills for managing phase III oncology clinical trials, focusing on efficiency, compliance, and quality from inception to completion.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Clinical Trial Management Course provides practical tools to manage efficient phase III oncology studies from start-up to closeout. Learn to optimise budgets, control costs, and track burn rates while safeguarding safety and data quality. Master RBM, monitoring strategies, CAPA design, site performance management, and data readiness to rescue timelines, support inspections, and deliver reliable results on schedule.
Elevify advantages
Develop skills
- Global trial governance: apply GCP, ICH, and ethics in oncology studies.
- Risk-based monitoring: design smart RBM plans and quality KPIs fast.
- Data readiness: manage EDC, queries, and interim database locks efficiently.
- Budget control: optimise CRO spend, forecasting, and cost-saving tactics.
- CAPA mastery: build effective CAPAs for deviations, consent, and data issues.
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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