Clinical Project Manager

vor 3 Wochen

Genève, Schweiz Teoxane SA Vollzeit

Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global patient care. Using its products, practitioners are able to fill all kinds of wrinkles, from the finest to the deepest, to restore youthful volume to the face, and to treat the neck and décolleté, with natural results. The strength of Teoxane is also its human size and independence. Teoxane has a total freedom of thoughts, action and innovation which makes the company unique.

In the frame of the growth of our business, we are looking for a:

Clinical Project Manager

Main activities

  • Implement, execute and complete clinical research project sponsored by Teoxane according to timelines and budget,
  • Be responsible of the compliance to local regulations, GCP regulations, and internal SOPs in clinical projects,
  • Able to work cross functionally within Teoxane departments to prepare required study documentations for submission to Ethic Committees and competent authorities which includes oversight, writing and review of documents,
  • 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 (i.e. from study protocol and study plans to final clinical study report) throughout the clinical study,
  • Responsible of the management of Contract Research Organizations (CROs) and third-party vendors and ensure adherence to scope of work within timelines and budget,
  • Able to work cross-functionally within the clinical team to monitor site performance (such as enrolment and compliance to study protocol), ensure high-quality data collection and review in clinical projects,
  • Ensure that all relevant documents are properly and timely archived in the TMF during the study,
  • Participate to the internal process improvements.

Your profile

  • Minimum B.Sc. degree in relevant scientific discipline e.g. Biochemistry, Microbiology, Pharmacy, Biological Sciences or Related Pharmaceutical Science,
  • 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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