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

• College/University degree or an equivalent combination of education, training & experience
• Life Science degree is a plus
• Administrative work experience, preferably in an international setting
• Prior experience in Clinical Research is a plus
• Full working proficiency in English, Kazakh and Russian
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication and collaboration skills

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.