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.

from 4 to 360h 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 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 to apply immediately for improving trial quality, controlling costs, and keeping studies on track.
Elevify advantages
Develop skills
- Mastery in trial budgeting: quickly estimate FTEs, site costs, and major vendors.
- Skills in vendor oversight: select, contract, and manage CROs, labs, and ePRO partners.
- Planning for oncology trials: 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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