(Senior) Clinical Research Associate

What you’d do

Conducts site monitoring visits (selection, initiation, routine, close-out) per GCP/ICH, builds relationships with investigative sites, and tracks enrollment, regulatory approvals, and data quality. Full time. 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