CRA 2, Oncology, IQVIA

What you’d do

Conduct on-site monitoring visits for oncology clinical trials, including selection, initiation, monitoring and close-out, ensuring sites follow GCP and ICH guidelines. Also train site staff, track subject recruitment, and escalate quality issues. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• 1.5+ years on-site oncology monitoring experience
• Site monitoring visits (selection, initiation, monitoring, close-out)
• Knowledge of GCP and ICH guidelines
• Protocol and study training for sites
• Subject recruitment tracking