Job Description
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 mattersPrepare draft regulatory/ethics submission dossierBe responsible for document management such as filing, processing, translation, quality control Update and maintain (automated) tracking systems, working files, and schedulesOrganize meetings, prepare agendas and minutesQualifications
College/University degree or an equivalent combination of education, training & experienceLife Science degree is a plusAdministrative work experience, preferably in an international settingPrior experience in Clinical Research i...