Clinical Trial Administrator I

  • Full time
  • Prague
  • Posted 2 weeks ago

Job Description

Start 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
  • Full working proficiency in English and CZ
  • 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 first step towards a career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.

    To apply for this job please visit