Regulatory Affairs Assistant

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