Job Description

Main Responsibilities:

  • Support the clinical operations team in managing trial documentation, site communication, and study supplies.
  • Maintain and update trial information in CTMS and eTMF systems.
  • Coordinate contracts, insurance certificates, and vendor-related activities.
  • Assist with SOP reviews, team meetings, and cross-functional collaboration.
  • Supporting in general documentations and administration 

    • Qualifications and Experience:

  • Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required;
  • Minimum 2 years of experience in clinical research – can have more, but not necessary.
  • Strong organizational and communication skills in English.
  • Proficient in MS Office and able to manage multiple priorities independently.
  • Detail-oriented, team player, and results-driven.

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