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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?

The Clinical Trials Management Course equips you with practical skills to conduct high-quality studies confidently. You will learn about investigator duties, ICH-GCP guidelines, sticking to protocols, and communicating with IRBs, then put into practice methods for scheduling visits, checking eligibility, obtaining informed consent, reporting safety issues, handling SAE processes, designing oncology trials for NSCLC, managing toxicity, conducting monitoring, audits, and ongoing quality improvements.

Elevify advantages

Develop skills

  • Clinical trial oversight: conduct GCP-compliant monitoring and audit programmes swiftly.
  • Safety reporting mastery: submit SAE reports and updates accurately and promptly.
  • Protocol operations: handle visits, labs, consent, and deviations precisely.
  • Oncology trial skills: use NSCLC criteria, RECIST fundamentals, and dosing modifications.
  • Toxicity management: respond quickly to hepatic and cardiac risks 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
Very great course. Lots of valuable information.
WiltonCivil Firefighter

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