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Medical Director

m/w/d, Basel-Stadt

Director RWE & Innovative Evidence is responsible for developing, supporting and implementing evidence strategies that deliver innovative and scientifically robust evidence to Therapeutic Areas (TAs) across the Innovative Medicine (IM) organization.

Responsibilities

Develop, drive and deliver on 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 internal change agent on matters pertaining to the overall creation and implementation of Innovative Medicines (IM) portfolio RWE / Integrated Evidence strategies and tactics.
Ask the right scientific questions, understand the evidence needs to optimize approval, access and clinical adoption of our medicines, and ideate and make recommendations on fit-for-purpose data and integrated evidence solutions.
Deliver high quality, rigorous, and fit-for-purpose evidence solutions according to Novartis priorities and opportunities to impact patients and society.
Closely collaborate with internal and external partners ensuring scientific rigor in evidence strategy, study design and analyses.
Contribute to partnerships with Medical Societies, Academic Institutes, payer bodies, other data owners to build meaningful RWD research collaborations.
Contribute to cross-functional, enterprise-wide and external evidence initiatives as well as to new and innovative data and analytic platforms, methodological approach-es 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).

Requirements

5+ years industry and/or relevant experience acquired at biopharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies
Strong 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.
Good understanding of drug development with proven ability to identify and deliver key evidence from retrospective and prospective studies to optimize regulatory approval, market access and clinical adoption.
Cross-functional experience working with Clinical Development, Commercial, Market Access, HEOR, Medical, Safety, and Regulatory colleagues.