Scientific Director- Medical

3 days ago

London, United Kingdom Cpl Life Sciences Full time

Director RWE & Innovative Evidence Hybrid - London
This role requires excellent scientific and technical expertise in real world data and observational research as well as a strong understanding of product and disease area strategies, our business, and healthcare environments. The Director RWE & Innovative Evidence will drive the development of integrated evidence approaches, techniques and standards as well as working closely with TAs, NIBR, GDD, Access and Medical and key countries to enable innovative evidence and sharing of best practices across geographies.

Act as a thought-leader and 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 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.
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 evidence 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 evi[1]dence to support product value demonstration aligned with local needs (patient access, reimbursement, medical education, and patient advocacy).
Key Performance Indicators (Indicate how performance for this job will be measured)
Timely creation of compelling and robust evidence, which support and enhances product development to optimize regulatory approval, patient access and clinical adoption in priority disease areas.
High quality integrated evidence plans (IEP) across the TAs and product lifecycle, which utilize best-in-class innovative approaches.
Consistent approach towards RWE generation, ensuring scientific rigor, aligned with RWE external and internal guidance.

MBA or equivalent preferred

Languages: English (oral and written)

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.
• Extensive industry experience generating evidence for assets across different stages of drug development.
• Strong external presence and connectivity, including an active network in RWE.
• Deep understanding of pharmaceutical value chain and its business processes.

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