Site Management Associate with Dutch

Experteer Overview
La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.
In this role you support the management and monitoring of clinical trial sites to ensure protocol adherence, regulatory compliance, and GCP standards. You will work with cross-functional teams to optimize site operations and data quality, and contribute to training and mentoring within the site management function. You’ll build strong relationships with site personnel while tracking performance and driving timely issue resolution. This is an opportunity to impact patient access to new medicines through efficient, compliant site management.
Compensaciones / Beneficios
• Coordinate monitoring activities at clinical trial sites ensuring protocol adherence and timely issue resolution
• Assist in preparing and reviewing Investigator Site File and Trial Master File documentation for GCP compliance...