Clinical Operations Manager


The Clinical Operations Manager is responsible for the organization, planning and follow-up of the operational aspects of a clinical trial/research project.

Main responsibilities

  • Support in the project development cycle with general tasks such as following up on requests to various partners, drafting guidelines, attend meetings and define actions for the COM activities (eg drug supply, translational research activities…)
  • Ensures adequate logistical and operational support to the study sites during start up and conduct of the project at any time
  • Ensure adequate project guidelines are maintained, and study-working book is updated in order to ensure continuity in situations of absence.
  • Update project tracking tools on an ongoing basis
  • Participate in project related meetings when applicable
  • Support in the redaction of the newsletters


  • Master’s degree in life sciences (biomedical sciences, pharmaceutical sciences…)
  • Team player who can work independently
  • Excellent communication skills
  • Able to prioritize adequately
  • Any previous experience in the clinical trials environment is an asset
  • Excellent knowledge of MS office tools
  • Fluent in English

Application form

*Compulsary fields
Application should be sent in English

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