Description

You will manage clinical study activities across multiple sites, focusing on medical devices. You'll oversee site performance, conduct company-initiated studies, and ensure quality through site visits and monitoring, working directly with a single sponsor while benefiting from the support of a global CRO.

Requirements

• Willingness to travel 50-80% to sites and surrounding countries
• Fluent in Dutch
• Prior experience in monitoring clinical trials and site management
• Bachelor's degree in scientific/medical discipline or equivalent
• Up to 8 years of experience as a CRA

Responsibilities

• Manage clinical study activities across multiple sites
• Oversee site performance and conduct company-initiated clinical studies
• Ensure high-quality deliverables through site visits and monitoring
• Maintain effective communication with sites and sponsor