CR
Clinical Research Associate
Check that a site followed the visit plan and the consent process.
A minute in the work
You read a visit schedule, then a note that a participant signed an older consent form. You write the facts, the process concern, and who should be told.
Competencies
Protocol visits
List visits, windows, and procedures.
Consent version control
Spot an outdated signature.
Source review
Compare the note with the plan.
Escalation
Name the documents to check before a conclusion.
Monitoring note
Write a factual follow-up.
Sample lab output
Watermarked sample. This is not your submission and it is not a reviewed score.
Open sample output