Role Description
The Senior Manager, Oncology, position within Medical Evidence Development (MED) Real-World Evidence & Epidemiology (RWE/Epi) provides an opportunity for a collaborative epidemiologist to support real-world evidence and epidemiologic studies as part of Medical strategy across the entire drug development process. The candidate will be responsible for:
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Synthesizing the literature and contributing to the design, conduct, and reporting of global epidemiologic research studies on Pfizer Oncology pipeline assets and approved products.
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Accountable for the quality, timeliness, and efficiency of all RWE/Epi deliverables in assigned product/disease area.
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Maintaining an internal network of Pfizer stakeholders to cultivate innovation, cross-functional collaboration, and identify new opportunities for RWE/Epi to increase the value of Pfizer assets.
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Developing external partnerships to leverage data resources and collaboration on high priority global studies.
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Authoring and reviewing study protocols, reports, and presentations.
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Communicating in writing and presentations to internal stakeholders, regulatory authorities, and medical professionals.
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Responsible for non-study deliverables such as RWE insights, epidemiology literature reviews, regulatory responses, and department initiatives.
This position will report directly to the Oncology Team Lead in RWE/Epi.
Qualifications
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PhD in Epidemiology, Statistics/Biostatistics, Health Outcomes Research, Quantitative Methods, Public Health, Health Economics, or Other Biological Science fields with a substantial quantitative component and at least 1 year of relevant experience in the pharmaceutical, academic and/or medical environment; or, MPH or another relevant Masterβs degree and at least 5 years of experience in the pharmaceutical, academic and/or medical environment, at least 1 of which were in the pharmaceutical industry.
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Demonstrated strong quantitative skills and methods expertise to generate rapid insights from real-world / observational data sources.
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Demonstrated strong technical writing skills and oral presentation skills with a track-record of publishing in peer-reviewed journals and presenting at medical/scientific conferences.
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Demonstrated ability to convert complex analysis into meaningful insights with data visualization and presentation tools and able to manipulate and analyze complex structured and unstructured data from multiple real-world evidence sources.
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Ability to work under pressure with a high level of autonomy/leadership on research projects and collaborate with multiple partners in a matrixed environment.
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Knowledgeable of the external regulatory environment for real-world evidence and maintains awareness of scientific developments in epidemiology, medicine, and technology (e.g., artificial intelligence).
Requirements
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Proficiency in rapid real-world data analytical platforms.
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Experience working with real-world data (RWD) including Electronic Medical Records (EMR), claims, and surveys.
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Excellent problem-solving and decision-making abilities.
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Ability to influence and collaborate with senior management and stakeholders.
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Strong project management skills with the ability to handle multiple projects simultaneously.
Benefits
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Work Location Assignment: Warsaw, Poland.
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Minimum annual gross base salary: 1,275,000 PLN.