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Clinical Research Management Course

Clinical Research Management Course
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

  • 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.
Workload: between 4 and 360 hours

What our students say

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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