Clinical Research Site Associate
Job Summary
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
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