Clinical Trial Administrator
PSI CRO
Warsaw, Masovian Voivodeship, PL
‎8 godz. temu

Job Description

Continue your career in clinical research, streamlining communication, maintaining systems and managing documents & information.

You will :

  • Be the point of contact for investigational sites, vendors, and multi-functional project teams
  • Be responsible for document management
  • Update and maintain (automated) tracking systems and schedules
  • Coordinate various activities within clinical research projects
  • Organize meetings, prepare agendas and minutes
  • Qualifications

  • College / University degree or an equivalent combination of education, training & experience
  • Administrative work experience, preferably in an international setting
  • Prior experience in Clinical Research is a plus
  • Full working proficiency in English and Polish
  • PC skills to be able to work with MS Word, Excel and PowerPoint
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication and collaboration skills
  • Additional Information

    Take your step towards a career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.

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