Clinical Research Site Associate

To support clinical research initiatives, the full-time Site Management Associate will streamline communication, maintain databases, and manage documentation while working remotely from anywhere in the Netherlands. Key responsibilities Maintain databases and tracking systems for clinical research projects Compile, procure, process, translate, and file large volumes of documents Serve as a communication point for investigative sites and coordinate query resolution and project training Required qualifications At least 6 months of experience in administrative and documentation management within clinical research Life Sciences university degree Full professional working proficiency in Dutch and English Proficiency in standard MS Office applications (Word, Excel, and PowerPoint) Good organizational and planning skills with a detail-oriented approach