Clinical Project Manager

vor 4 Wochen


Genf, Genf, Schweiz Teoxane SA Vollzeit
Main Responsibilities:
  • Lead clinical research projects sponsored by Teoxane SA according to timelines and budget.
  • Ensure compliance to local regulations, GCP regulations, and internal SOPs in clinical projects.
  • Collaborate with cross-functional teams to prepare required study documentations for submission to Ethic Committees and competent authorities.
  • Develop and manage the overall clinical study budget.
  • Select and validate investigator/site, and vendors (i.e CROs).
  • Contribute to the negotiation and preparation of contracts and budgets with third parties and sites participating in our studies.
  • Responsible of the development of high-quality study documentation throughout the clinical study.
  • Manage Contract Research Organizations (CROs) and third-party vendors to ensure adherence to scope of work within timelines and budget.
  • Monitor site performance, ensure high-quality data collection and review in clinical projects.
  • Ensure proper archival of relevant documents in the TMF during the study.
  • Requirements:
    • Minimum B.Sc. degree in a relevant scientific discipline.
    • Minimum of 4 years of experience in clinical operations; project management skills.
    • Experience in industry, especially in medical device clinical trials is a plus.
    • Strong critical thinking and problem solving skills.
    • Strong negotiation, communication and presentation skills across all levels.
    • Able to rapidly adapt to changing environment and circumstances.
    • Fluent in English and French.


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