from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Clinical Trials Management Course gives you practical skills to run high-quality studies with confidence. Learn investigator responsibilities, ICH-GCP, protocol adherence, and IRB communication, then apply hands-on methods for visit scheduling, eligibility checks, informed consent, safety reporting, SAE workflows, oncology trial design for NSCLC, toxicity management, monitoring, audits, and continuous quality improvement.
Elevify advantages
Develop skills
- Clinical trial oversight: run GCP-compliant monitoring and audit programs fast.
- Safety reporting mastery: file SAE reports and updates accurately and on time.
- Protocol operations: manage visits, labs, consent, and deviations with precision.
- Oncology trial skills: apply NSCLC criteria, RECIST basics, and dosing adjustments.
- Toxicity management: act quickly on hepatic and cardiac risks in trial patients.
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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