Sr. CRA 1, IQVIA

What you’d do

Monitor clinical trial sites through selection, initiation, monitoring, and close-out visits per Good Clinical Practice. Train site staff, track subject recruitment, and evaluate data quality and protocol compliance. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Bachelor's in scientific discipline or health care preferred
• 2+ years on-site monitoring experience
• Knowledge of clinical research regulatory requirements
• Site monitoring visits per GCP