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 of flexible workload
certificate valid in your country
What Will I Learn?
The Clinical Research Management Course equips you with practical skills to plan and execute complex phase III oncology trials confidently. You will learn protocol fundamentals, realistic timelines, enrolment projections, resource and budget planning, vendor selection and supervision, risk management, and governance. Acquire clear, actionable tools to apply right away for enhancing trial quality, managing costs, and ensuring studies stay on schedule.
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
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