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Clinical Research Associate Course

Clinical Research Associate Course
flexible workload of 4 to 360h
valid certificate in your country

What will I learn?

This course offers hands-on, step-by-step guidance for Clinical Research Associates to monitor clinical trials effectively and in full compliance. Key topics include designing CAPA plans, reviewing informed consent forms, performing source data verification for data integrity, conducting eligibility assessments, identifying and reporting serious adverse events, and managing investigational medicinal product accountability. Participants will develop skills in creating inspection-ready documents using standard templates, SOP-driven procedures, and focused monitoring techniques right from the start.

Elevify advantages

Develop skills

  • SAE safety oversight: swiftly detect, record, and report serious adverse events.
  • IMP accountability: manage drug inventory reconciliation, returns, storage, and temperature controls.
  • Eligibility verification: validate inclusion criteria and address source data discrepancies.
  • CAPA execution: formulate, document, and monitor corrective and preventive actions.
  • Informed consent review: check timing, signatures, and ensure full documentation compliance.

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.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor of the Prison System, and the course from Elevify was crucial for me to be chosen.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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