Tech Stack

Description

You will manage clinical study activities across multiple sites for medical device studies, oversee site performance, and ensure high-quality deliverables through site visits and monitoring. This role offers the stability and career growth of a global CRO while working directly with leading pharmaceutical companies in Germany.

Requirements

• Prior experience in monitoring clinical trials and site management
• Willingness to travel 50-80%
• Fluent in German required
• Bachelor's degree in scientific, medical, or paramedical discipline
• Up to 8 years of experience as a CRA

Responsibilities

• Manage clinical study activities across multiple sites
• Conduct company-initiated clinical studies with focus on medical devices
• Oversee site performance and ensure high-quality deliverables
• Perform site visits and monitoring
• Communicate effectively with sites and project teams