from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Clinical Trials Management Course provides practical skills to conduct high-quality studies with assurance. You will learn about investigator duties, ICH-GCP guidelines, sticking to protocols, and communicating with IRBs, then use practical 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 correctly and promptly.
- Protocol operations: handle visits, labs, consent, and deviations accurately.
- Oncology trial skills: use NSCLC criteria, RECIST fundamentals, and dosing modifications.
- Toxicity management: respond fast to liver and heart risks in trial patients.
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.What our students say
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