Clinical Trials Management Course
Gain expertise in managing clinical trials, especially oncology and NSCLC studies. Master ICH-GCP guidelines, SAE management, site monitoring, protocol compliance, and handling hepatic and cardiac toxicities confidently in practical medical settings. This course builds essential skills for running high-quality trials effectively.

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.What our students say
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