Clinical Trial Management Course
This course equips professionals with essential skills to manage clinical trials effectively, focusing on oncology phase III studies, from budgeting and risk management to data quality and regulatory compliance.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Clinical Trial Management Course provides practical tools to run efficient phase III oncology studies from start-up to closeout. Learn to optimize budgets, control costs, and track burn rates while protecting safety and data quality. Master RBM, monitoring strategies, CAPA design, site performance management, and data readiness so you can 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: optimize 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 the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students are saying
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