Clinical Research Management Course
This course provides hands-on training in managing clinical research, focusing on oncology trials, budgeting, vendor management, planning, risk assessment, and governance to ensure efficient and compliant 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 execute complex phase III oncology trials with assurance. You will learn protocol fundamentals, realistic timelines, enrolment projections, resource and budget estimations, vendor selection and supervision, risk management, and governance. Acquire straightforward, practical tools you can use right away to enhance trial quality, manage costs, and ensure studies stay on course.
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
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