Job title:
Clinical Development Lead Oncology (m/f/d)
Company
Work Selection
Job description
TemporärJobregion: Rotkreuz, SchweizStellenprozente: 100 %Pharma & Chemie & Life ScienceClinical Development Lead Oncology (m/f/d)BeschreibungFor our international medical partner, Roche Diagnostics Int Ltd. based in Rotkreuz, we are looking for a qualified and motivated Clinical Development Lead Oncology for one year with option for extension.The Clinical Development Lead Oncology is responsible for planning and implementation of Clinical Development activities for novel medical value diagnostic solutions in the areas of Chronic Liver Diseases at Roche Diagnostic Solutions (RDS), with a primary focus on Liver fibrosis. The Clinical Development Lead will contribute to the development and implementation of Roche Diagnostics long-term, medical value strategy and pipeline.Tasks
- Serve as a subject matter expert for Liver Oncology, clinical study design and evidence generation strategies for internal and external stakeholders in the assigned indication area
- Responsible for critical review of study results, protocol and report generation to support new product development
- Works with colleagues from Business, Medical Affairs, Clinical Operations, Regulatory Affairs, Biometrics, Development, Quality, and other functions to ensure appropriate implementation of clinical development strategies
- Builds and maintains strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, in meeting business goals and ensuring operational excellence
- Act as an ambassador and representative of Clinical Development establishing effective collaborative relationships with key functions for new and existing products, incl. clinical utility, intended use and claim extensions
- Play a leadership role in maintaining clinical, regulatory, and scientific expertise as it relates to IVD product development and regulatory documentation. Leads medical/scientific input and preparation of regulatory submissions as well as responses to reviewers from regulatory agencies
- Drives competitive differentiation, innovation and early pipeline activities and develops intellectual property strategy
- Responsible for comprehensive literature reviews, supervises collation of relevant clinical and scientific information from different sources, and creates new scientific content (without guidance/direction)
- Demonstrate leadership skills; ability to mentor and provide an environment for personal and professional growth
Must Haves
- Medical degree or advanced degree in Life Sciences (PhD, PharmD or equivalent degree) with relevant expertise in the Healthcare Industry and/or academic institutions
- Min. 2-3 years of industry experience after PhD or coming straight from the industry with at least 5+ years of experience in IVD
- Strong experience in liver Indication (Fibrosis and/or Liver cancer)
- Min. 5+ years academic, diagnostics or pharma industry experience, preferably, having experience in IVD or Medical Device development in all stages of global studies, development of study protocol design, report writing and leading matrixed teams
- Ability to lead clinical development studies/programs and good knowledge in applicable standards and regulations (ICH-GCP, IVDD/IVDR, MDR, FDA, NMPA regulations etc.) especially in global studies in the US and negotiation with the FDA
- Understands agile culture and exhibits an agile mindset. Embraces the VACC (Visionary, Architect, Coach, Catalyst) principles, fosters excellence and enables a productive and collaborative work environment
- Excellent verbal and written communication, presentation and negotiation skills in English
- Demonstrate flexibility and adaptability to perform in a fast-paced, matrixed environment where fluid, cross-team collaboration is crucial
- Excellent analytical skills and strategic mindset.
- Ability to work independently
Are you interested? Do not hesitate and submit your complete application documents online today.We also process applications by post, but will not return them for administrative reasons. We look forward to hearing from you!Wir wertschätzen Vielfalt und begrüssen daher alle Bewerbungen – unabhängig von Geschlecht, sozialer Herkunft, Religion, Alter und Identität. Zur leichteren Lesbarkeit und besseren Verständlichkeit verwenden wir nur eine Gender-Form. Selbstverständlich sind im jeweiligen Kontext alle Genderformen gleichermassen gemeint.
Expected salary
Location
Rotkreuz, Zoug
Job date
Fri, 31 Jan 2025 00:50:39 GMT
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