Conduct site visits (initiation, monitoring, close-out) and keep sites aligned with protocol and GCP.
Verify source data and help resolve queries quickly.
Provide training and serve as a go-to for site staff.
Enter and review clinical data in EDC.
Spot issues and inconsistencies early and follow through to resolution.
Help keep data flowing on time and accurate.
Support study start-up (reg docs, IRB/EC submissions, site set-up).
Maintain study files and trackers (eTMF, logs, spreadsheets).
Track enrollment, timelines, and key milestones.
Jump in wherever needed — from vendor coordination to preparing reports for leadership.

Clinical Research Associate / Clinical Ops Coordinator

Key skills