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Clinical Trials Management Course

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

What will I learn?

This course imparts practical skills for managing clinical trials confidently. You will learn investigator duties, ICH-GCP standards, protocol compliance, and IRB interactions. Hands-on training covers visit scheduling, eligibility screening, informed consent processes, safety reporting, SAE procedures, NSCLC oncology trial design, toxicity control, monitoring, audits, and ongoing quality enhancement in clinical research.

Elevify advantages

Develop skills

  • Clinical trial oversight: conduct GCP-compliant monitoring and audit programmes efficiently.
  • Safety reporting mastery: submit SAE reports and updates accurately and promptly.
  • Protocol operations: handle visits, labs, consent, and deviations precisely.
  • Oncology trial skills: implement NSCLC criteria, RECIST basics, and dosing adjustments.
  • Toxicity management: respond swiftly to hepatic and cardiac risks in trial patients.

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 of 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
Very great course. Lots of rich information.
WiltonCivil Firefighter

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