Clinical Scientific Project Manager

vor 1 Woche


Home Office, Schweiz Thermo Fisher Scientific Vollzeit

**Key Responsibilities**:

- Coordinate projects beginning to generate supporting evidence for NGS utilization in Oncology (Clinical Validity/Utility studies);
- Develop and facilitates investigator sponsored trial/studies while supervising progress and adherence to timelines, commitments, results and obligations approved projects;
- Support the design of studies with collaborators to ensure rapid adoption of the Oncoming solutions and ensure partnership between Thermo Fisher Scientific and partner scientists/clinicians to meet the aims and successful outcome of the partnership.
- Interact appropriately with healthcare professionals, clinical investigators, and customers in order to provide accurate, balanced, scientifically detailed and information.
- Scientific Meeting Coverage: provide affairs coverage of medical/ congresses and coordinated group meetings as needed. Listen for and interpret new clinical data as part of a continuous competitive intelligence monitoring process, report on findings to medical affairs and marketing internal customers,
- Stay ahead of the clinical literature in NGS specifically in Oncology and Pathology;
- Be accountable for the quality and consistency of scientific and medical knowledge of the Medical Affairs Team.

**Minimum Requirements/Qualifications**:

- Holds a PhD in scientific/medical sciences;
- A minimum of 3+ years’ experience in the pharmaceutical, medical device, or diagnostics industry;
- Alternatively, 3+ years’ experience in routine clinical molecular diagnostics (including consultancy and/or academia);
- A strong scientific background in Oncology, haemato-oncology preferred;
- Must be a teammate with problem-solving and strategic influencing skills;
- Requires the ability to efficiently articulate highly technical/sophisticated scientific data and concepts to audiences with differing scientific and technical knowledge;
- Must have consistent record to perform efficiently under stringent timelines and with changing and adventurous priorities;
- Understands factors driving market access and how clinical evidence can support access decisions;
- International experience is required, as well as validated cultural diversity awareness;
- Proficiency in English with additional language desirable;
- Ability to travel at least 30%, while working from remote within EU.



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