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'll learn about investigator duties, ICH-GCP guidelines, sticking to protocols, and liaising with IRBs, then put into practice hands-on approaches for scheduling visits, verifying eligibility, obtaining informed consent, reporting safety issues, handling SAE processes, designing oncology trials for NSCLC, managing toxicity, conducting monitoring, audits, and ongoing quality enhancements.
Elevify advantages
Develop skills
- Clinical trial oversight: swiftly manage GCP-compliant monitoring and audit programmes.
- 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 rapidly 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.What our students say
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