from 4 to 360h flexible workload
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 efficiently.
- 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 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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