Careers @ DICE

Medical Writer


As a Medical Writer, you will be responsible for writing, editing, and finalizing project documents.

This involves:

  • Writing clinical study reports (CSR)
  • Writing clinical study protocols
  • Writing protocol amendments
  • Preparation of journal manuscripts
  • Creation of posters and presentations



  • Master's degree or PhD in Science, preferably in a biological- or medical-related field


  • 3 years of experience with scientific writing
  • Experience with the conduct of clinical trials is a plus


  • Excellent verbal and written skills in English - knowledge of Dutch or French is a plus
  • Excellent knowledge of MS Office
  • Excellent organizational and time management skills
  • Excellent communication and problem-solving skills

Key competencies
  • Flexibility to engage in a variety of tasks
  • Eagerness to learn and continuously develop
  • Resistance to stress
  • Eye for detail
  • Respect for deadlines
  • Customer focus
  • Achievement-orientation
  • Conceptual thinking
  • Integrity and trustworthiness

Join the DICE team!

Check out our current team.