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 investigator duties, ICH-GCP guidelines, protocol compliance, and IRB interactions, then practise 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 enhancement.
Elevify advantages
Develop skills
- Clinical trial oversight: conduct GCP-compliant monitoring and audit programmes swiftly.
- Safety reporting mastery: submit SAE reports and updates precisely and promptly.
- Protocol operations: handle visits, labs, consent, and deviations accurately.
- Oncology trial skills: utilise 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 workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workloadWhat our students say
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