Clinical Research — CRA Starter

GCP, monitoring and site documentation skills employers screen for.

What you'll be able to do

• • Apply ICH-GCP principles to real monitoring scenarios
• • Review essential documents and a trial master file
• • Handle a protocol deviation professionally

Track steps

1. Roadmap~10h

   Clinical Research roadmap — regulatory basics

   ICH-GCP, ethics committees, informed consent.

   Open
2. Academy course~10h

   Academy: monitoring visits end to end

   Pre-study, initiation, routine and close-out.

   Open
3. Hands-on project~6h

   Write a monitoring visit report from a case scenario

   Findings, action items and escalation.

4. Mentor checkpoint~1h

   Mentor checkpoint — report critique

   A working CRA reviews your report line by line.

   Open
5. Academy course~5h

   Academy: interview prep for CRA roles

   Competency questions and scenario answers.

   Open
6. Mentor checkpoint~1h

   Final checkpoint — mock interview

   Scored mock interview and credential sign-off.

   Open