Clinical Trials Management Course
Gain expertise in clinical trials management for oncology and NSCLC. Apply ICH-GCP guidelines, manage serious adverse events, monitor sites effectively, ensure strict protocol adherence, and confidently handle hepatic and cardiac toxicities in real-world medical settings. This course equips you with practical skills for high-quality study execution.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This course imparts practical skills for managing clinical trials confidently. You will learn investigator duties, ICH-GCP standards, protocol compliance, and IRB interactions. Hands-on training covers visit scheduling, eligibility screening, informed consent processes, safety reporting, SAE procedures, NSCLC oncology trial design, toxicity control, monitoring, audits, and ongoing quality enhancement in clinical research.
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 basics, and dosing adjustments.
- Toxicity management: respond swiftly to 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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