Join our international team and support regulatory aspects of clinical research projects, streamlining communication, maintaining electronic systems and managing documents.
Office-Based in Belgrade, Serbia
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 and Serbian
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication and collaboration skills
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
