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Clinical Trials Management Course

Clinical Trials Management Course
4 to 360 hours of 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. You will learn about investigator responsibilities, ICH-GCP guidelines, protocol compliance, and IRB interactions, followed by hands-on approaches to visit scheduling, eligibility screening, informed consent processes, safety reporting, SAE procedures, oncology trial design for NSCLC, toxicity handling, monitoring, audits, and ongoing quality enhancement.

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 fundamentals, and dosing modifications.
  • Toxicity management: respond swiftly 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 the chosen one.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Great course. Lots of valuable information.
WiltonCivil Firefighter

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