Clinical Research Associate

Role Overview

• Conduct site monitoring for clinical trials
• Provide oversight and guidance for clinical trial management
• Collaborate with cross-functional teams to ensure protocol compliance

Requirements

• Bachelor’s degree in a relevant field (sciences, nursing, medical preferred)
• Experience in the pharmaceutical, health care, biotech, medtech or CRO industries
• Strong command of English, and the local language as necessary, both written and verbal.
• Willing and able to travel up to 85% to support site visits and project needs.

Benefits

• Professional development
• Global travel
• Flexible work programs