from 4 to 360h 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. Learn investigator duties, ICH-GCP, protocol compliance, and IRB liaison, then practise hands-on approaches for visit planning, eligibility screening, informed consent, safety notifications, SAE processes, oncology trial setup for NSCLC, toxicity handling, monitoring, audits, and ongoing quality enhancement.
Elevify advantages
Develop skills
- Clinical trial supervision: conduct GCP-compliant monitoring and audit programmes swiftly.
- Safety reporting expertise: submit SAE reports and updates precisely and promptly.
- Protocol management: oversee visits, labs, consent, and deviations accurately.
- Oncology trial abilities: utilise NSCLC criteria, RECIST fundamentals, and dosage modifications.
- Toxicity control: respond rapidly to hepatic and cardiac hazards 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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Course in PDF
