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Clinical Trials Management Course

Clinical Trials Management Course
from 4 to 360h flexible workload
certificate valid in your country

What will I learn?

The Clinical Trials Management Course equips you with practical skills to conduct high-quality studies confidently. Learn investigator duties, ICH-GCP, protocol compliance, and IRB liaison, then practise hands-on approaches for visit planning, eligibility screening, informed consent, safety notifications, SAE processes, oncology trial setup for NSCLC, toxicity handling, monitoring, audits, and ongoing quality enhancement.

Elevify advantages

Develop skills

  • Clinical trial supervision: conduct GCP-compliant monitoring and audit programmes swiftly.
  • Safety reporting expertise: submit SAE reports and updates precisely and promptly.
  • Protocol management: oversee visits, labs, consent, and deviations accurately.
  • Oncology trial abilities: utilise NSCLC criteria, RECIST fundamentals, and dosage modifications.
  • Toxicity control: respond rapidly to hepatic and cardiac hazards in trial participants.

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

I was just promoted to Intelligence Advisor for the Prison System, and the course from Elevify was crucial for me to be chosen.
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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Course in PDF