Clinical Research Management Course
This course provides hands-on training in managing phase III oncology trials, covering protocol development, timelines, budgeting, vendor management, risk assessment, and governance to enhance trial efficiency and compliance.

flexible workload from 4 to 360h
valid certificate in your country
What will I learn?
The Clinical Research Management Course equips you with practical skills to plan and manage complex phase III oncology trials confidently. You will learn protocol essentials, realistic timelines, enrolment forecasting, resource and budget estimation, vendor selection and oversight, risk management, and governance. Gain clear, actionable tools you can apply right away to boost trial quality, control costs, and keep studies on track.
Elevify advantages
Develop skills
- Trial budgeting mastery: quickly estimate FTEs, site costs and major vendors.
- Vendor oversight skills: select, contract and manage CROs, labs and ePRO partners.
- Oncology trial planning: design realistic phase III timelines and enrolment curves.
- Risk-based operations: build and run a live risk register for global oncology studies.
- Governance and reporting: lead study meetings and create clear, audit-ready dashboards.
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
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course workload?
What are the courses like?
How do the courses work?
What is the duration of the courses?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
PDF Course