Medical Director (m/f/d)
- Develop and drive overarching innovative integrated evidence strategies, in collaboration with internal partners, to ensure that the value of our medicines is fully supported by evidence
- Act as a thought-leader and internal change agent on matters pertaining to the over-all creation and implementation of RWE / Integrated Evidence strategies and tactics
- Ask the right scientific questions, understand the evidence needs to optimize ap-proval, access and clinical adoption of our medicines, and ideate and make recom-mendations on fit-for-purpose data and integrated evidence solutions
- Deliver high quality, rigorous, and fit-for-purpose evidence solutions according to Company priorities and opportunities to impact patients and society
- Closely collaborate with internal and external partners ensuring scientific rigor in ev-idence strategy, study design and analyses
- Lead partnerships with Medical Societies, Academic Institutes, payer bodies, other data owners to build meaningful RWD research collaborations. Lead or contribute significantly to cross-functional, enterprise-wide and external evi-dence initiatives as well as to new and innovative data and analytic platforms, methodological approaches and technologies, which enable broader and more effective use of integrated evidence to reimagine medicine
- Work closely with key countries to develop timely, meaningful and robust evidence to support product value demonstration aligned with local needs (patient access, re-imbursement, medical education, and patient advocacy)
- Define and deliver on goals and objectives, identify opportunities, gaps and priorities, and contribute to best practice standards
- Ensure appropriate prioritization of funding and resources, informed by trade-off, valuation analysis where appropriate and aligned with TA strategy. Stay abreast of emergent applications, external insights, trends and requirements, and internal learnings, and positively drive development of innovative evidence
- Develop strong internal and external partnerships to promote effective collaborations. Lead by example in promoting a collaborative and entrepreneurial culture and mindset. Be an advocate and champion by engaging support for innovative ideas and solutions and ensuring a broad understanding of the value of RWE and integrated evidence to the product value demonstration both globally and in key markets.
- Solid industry and/or relevant experience acquired at biopharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies
- Deep understanding and experience of RWD/RWE and/or related disciplines to generate scientifically rigorous and impactful evidence, both from prospective and retrospective studies, including secondary data sources
- Strong understanding of drug development with proven ability to identify and deliver impactful evidence from retrospective and prospective studies to optimize regulatory approval, market access and clinical adoption
- Strong cross-functional experience working with Clinical Development, Commercial, Market Access, HEOR, Medical, Safety, and Regulatory colleagues
- Deep understanding of and experience with research methodology and statistical methods related to retrospective and prospective clinical data analysis, and observational and/or epidemiological research
- Demonstrated track record leading and executing research projects using RWD from claims, electronic health records, registries, biobanks, or digital applications, including publications
- Considerable experience in collaborating with quantitative scientists and analysts
- Strong leadership skills, with an ability to motivate and inspire teams and manage change
- Proven ability to develop and successfully implement new strategies and ideas
- Strong communication skills. Proven ability to translate and effectively communicate complex technical concepts and innovative evidence solutions to diverse audiences
- Very renowned Pharmaceutical Company
- International Environment
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