Regulatory Affairs Assistant
Job Location:
Almaty - Kazakhstan
Monthly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
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
Qualifications :
- 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
Additional Information :
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.
Remote Work :
No
Employment Type :
Full-time
About Company
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on on-time project delivery. This is achieved through investing substantial effo ... View more
