Group 10

  • To manage clinical and regulatory documentation in a Documentum-based system (Pluto)
  • To ensure the electronic integrity of the documentation and compliance with internal and external standards and requirements
  • To assist in the production of documents
  • To perform format quality control of these documents
  • To manage the clinical parts of the Submission Index

Group 12

  • You have already worked in the filed of clinical trials
  • Skilled user of EDMS (Pluto), Word high level superuser, PDF formatting
  • Very good English communicator
  • Flexibility for travelling to Denmark


Clinical Submission Coordinator 495