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Clinical Research Project Manager Training

Clinical Research Project Manager Training
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

This training delivers hands-on skills for managing oncology clinical trials efficiently from initiation to completion. Cover site selection, IRB processes, enrolment strategies, budgeting, cost management, governance, and risk-based monitoring. Acquire templates, tools, and workflows to enhance timelines, data accuracy, safety, and trial success in a targeted format.

Elevify advantages

Develop skills

  • Master site start-up: speed up feasibility checks, IRB approvals, and site activation.
  • Design Phase II oncology trials: create efficient, FDA-compliant colorectal cancer studies.
  • Optimise enrolment: predict rates, increase accrual, and handle weak sites.
  • Control budgets: develop, negotiate, and adjust costs for complex oncology trials.
  • Oversee quality and safety: use risk-based monitoring, CAPA, and pharmacovigilance for audits.

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.
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 I work for.
SilviaNurse
Great course. A lot of valuable information.
WiltonCivil Firefighter

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