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.