4 to 360 hours of flexible workload
certificate valid 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 responsibilities, ICH-GCP guidelines, protocol compliance, and IRB interactions, followed by hands-on approaches to visit scheduling, eligibility screening, informed consent processes, safety reporting, SAE procedures, oncology trial design for NSCLC, toxicity handling, monitoring, audits, and ongoing quality enhancement.
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: implement 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 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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