Precision Medicine Leader Oncology
vor 1 Tag
**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.**
**Precision Medicine Leader Oncology M/F/d**
**YOUR TASKS AND RESPONSIBILITIES**
- Act as Precision Medicine leader (PML) for development of one or more programs. Responsible for defining and delivering OPM strategy and for providing strategic, clinical, scientific, technical and budgetary input for assigned projects. Act as an equal member of the Translational Science sub team. Provide relevant Oncology expertise to Translational Science sub team and Clinical Development Teams.
- Act as thought partner to research leaders for pre-IND programs. Proactively follow early projects and take an active role in discovering novel biomarkers and performing preclinical validation studies. Draw on resources from across the organization to ensure delivery of a biomarker strategy.
- Ensure coordination of all aspects of biomarker discovery, development, validation, and clinical implementation in synchronization with the drug R&D process. Leverage cutting-edge methodologies to enable biomarker strategy.
- Represents biomarker related aspects internally and externally at conferences, with authorities and ethics committees, and with external key opinion leaders. Builds and maintain a network with academic institutions and diagnostic companies in Oncology. Work closely with external clinical leaders to ensure successful uptake of biomarker strategy in the clinic.
- Lead, via internal and external collaborations, the development of patient selection and surrogate response biomarker endpoint.
- Ensure regulatory compliance of biomarker activities and drive biomarker qualification processes.
- Independently analyze, interpret, and present results from biomarker analyses and draw conclusions that support and enable decision making.
**WHO YOU ARE**
- Medical doctor (MD), PhD, or MD/PhD in Biochemistry, Molecular Biology, or Genetics or similar
- Proven track record of clinical development, preferably in Oncology, incl. several years of industry experience
- Understanding of disease pathophysiology and current therapeutics in oncology
- Focus on early-stage drug development, including experience implementing biomarkers in Phase I, regulatory framework for bio sampling, and translational medicine in Oncology
- Strong scientific reputation as evidenced by multiple publications in peer reviewed journals and as speaker of conferences
- Strong network in the academic and clinical community of Oncology
- Strong leadership skills, comfortable to marshal resources from different parts of the organization
- Companion Diagnostic experience preferred
LI-GH
**YOUR APPLICATION**
**Location**:
Switzerland : Basel-City : Basel
**Division**:
Pharmaceuticals
**Reference Code**:
794857
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