Clinical Research Management Course
This course provides essential skills for managing clinical research, focusing on oncology trials, including budgeting, vendor management, planning, risk assessment, and governance to ensure efficient and high-quality study execution.

4 to 360 hours flexible workload
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 with confidence. You'll 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 straight 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 the 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 come with a certificate?
Are the courses free?
What is the duration of the courses?
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 online course and how does it work?
PDF Course