Clinical Research Associate

What you’d do

Monitors and supports clinical study sites, conducting qualification, initiation, interim monitoring and closeout visits to protect participant safety and data integrity. Serves as liaison between sponsor and sites on protocol, regulatory compliance and data collection. Full time. Found on the employer's careers page on Oct 17, 2026. Apply through the link.

You’ll need

• Knowledge of GCP and clinical research regulations
• Site monitoring experience (qualification, initiation, closeout)
• Source data verification and adverse event reporting
• Excellent verbal, written, and interpersonal communication skills
• Cross-functional collaboration