Join our international team and support regulatory aspects of clinical research projects, streamlining communication, maintaining electronic systems and managing documents.
Full-time employment based in Almaty, Kazakhstan
You will:
- Be the point of contact for clinical project teams and support services on regulatory matters
- Prepare draft regulatory/ethics submission dossier
- Be responsible for document management such as filing, processing, translation, quality control
- Update and maintain (automated) tracking systems, working files, and schedules
- Organize meetings, prepare agendas and minutes