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Clinical Trials Management Course

Clinical Trials Management Course
flexible workload from 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 hands-on approaches 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 improvement.

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 basics, and dosing adjustments.
  • Toxicity management: respond quickly to hepatic and cardiac risks in trial patients.

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 selected.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of valuable information.
WiltonCivil Firefighter

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