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Clinical Trials Management Course

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

What will I learn?

This course equips you with practical skills to manage clinical trials confidently. You will learn investigator duties, ICH-GCP standards, protocol compliance, IRB interactions, and hands-on techniques for scheduling visits, screening eligibility, obtaining informed consent, reporting safety issues, handling SAEs, designing oncology trials for NSCLC, managing toxicities, conducting monitoring and audits, and improving quality continuously.

Elevify advantages

Develop skills

  • Clinical trial oversight: conduct GCP-compliant monitoring and audits efficiently.
  • Safety reporting expertise: submit SAE reports and updates accurately and promptly.
  • Protocol management: handle visits, labs, consent, and deviations precisely.
  • Oncology trial proficiency: use NSCLC criteria, RECIST principles, and dosing changes.
  • Toxicity control: respond swiftly to hepatic and cardiac risks in trial participants.

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

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 my boss's and the company's expectations.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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