(Senior) Clinical Research Associate, IQVIA

What you’d do

Monitor clinical trial sites through selection, initiation, routine, and close-out visits, ensuring GCP compliance, data integrity, and enrollment progress. Full time, collaborating with investigative sites and cross-functional teams. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Bachelor's in life sciences, healthcare, or related field
• 1.5+ years of on-site monitoring experience
• Knowledge of GCP, ICH, and regulatory requirements
• Strong communication and organizational skills
• Ability to manage multiple priorities