Senior Site Management Coordinator
Reading, UK
3d ago


  • Assist the team in the preparation, handling, distribution, filing and archiving of documentation
  • Review documents for completeness, consistency and accuracy, under guidance of senior staff
  • Prepare client deliverable documents using appropriate tools and draft text for straightforward documents, under guidance of senior staff
  • Completion of relevant Clinical Trial Management System (CTMS) fields, databases, tracking tools, timelines and project plan with project specific information
  • Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers
  • Interact with internal and external clients, under guidance of senior staff
  • Perform IP release activities on small, straightforward projects or support reviews for larger projects
  • Requirements

  • Strong word processing skills and knowledge of MS Office applications.
  • General awareness clinical trial environment and drug development process.
  • Ability to work on multiple projects.
  • Apply
    Add to favorites
    Remove from favorites
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Application form