Senior Manager, MED Oncology RWE/Epi Scientist

Pfizer

. Support real-world evidence and epidemiologic studies as part of Medical strategy across the entire drug development process .

Posted 10/8/2026full-timeRemote • PolandSenior💰 PLN 1,275,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Epidemiology and strong quantitative skills to generate insights from real-world evidence. Proficient in technical writing, data visualization, and collaboration within a matrixed environment to support global regulatory submissions.

Highest-signal resume keywords

PhD In EpidemiologyStrong Quantitative SkillsTechnical WritingData VisualizationRegulatory Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Epidemiologic ResearchData AnalysisStatistical MethodsReal-World EvidenceHealth Outcomes ResearchBiostatisticsQuantitative MethodsResearch Protocol DevelopmentScientific WritingPresentation Skills

Soft Skills

CollaborationLeadershipCommunicationAutonomyProblem-Solving

Tools & Technologies

Data Visualization ToolsPresentation SoftwareStatistical Software

Industry Keywords

Pharmaceutical IndustryRegulatory SubmissionsFDAEMAObservational DataMatrixed EnvironmentPeer-Reviewed JournalsMedical ConferencesScientific DevelopmentsArtificial Intelligence

About the role

Key responsibilities & impact

Support real-world evidence and epidemiologic studies as part of Medical strategy across the entire drug development process
Synthesize literature and contribute to the design, conduct, and reporting of global epidemiologic research studies on Pfizer Oncology pipeline assets and approved products
Ensure the quality, timeliness, and efficiency of RWE/Epi deliverables in the assigned product/disease area
Maintain an internal network of Pfizer stakeholders to cultivate innovation, cross-functional collaboration, and new RWE/Epi opportunities
Develop external partnerships to leverage data resources and collaborate on high-priority global studies
Author and review study protocols, reports, and presentations
Communicate in writing and presentations with internal stakeholders, regulatory authorities, and medical professionals
Deliver non-study outputs including RWE insights, epidemiology literature reviews, regulatory responses, and department initiatives
Partner with Chief Medical Office colleagues to address asset-team evidence needs and support global regulatory submissions to the FDA, EMA, and other agencies
Deliver rapid insights from real-world observational data sources
Develop presentations, webinars, manuscripts, scientific data packages, and other communication materials
Assure quality, compliance, and management of research activities
Participate in peer review of RWE/Epi study protocols and reports
Document requests and track progress toward project completion, metrics, and business goals
Report directly to the Oncology Team Lead in RWE/Epi

Requirements

What you’ll need

PhD in Epidemiology, Statistics/Biostatistics, Health Outcomes Research, Quantitative Methods, Public Health, Health Economics, or another biological science field with a substantial quantitative component and at least 1 year of relevant experience in the pharmaceutical, academic and/or medical environment; or an MPH or another relevant Master’s degree and at least 5 years of experience in the pharmaceutical, academic and/or medical environment, including at least 1 year in the pharmaceutical industry
Strong quantitative skills and methods expertise for generating rapid insights from real-world/observational data sources
Strong technical writing and oral presentation skills, with a track record of publishing in peer-reviewed journals and presenting at medical/scientific conferences
Ability to convert complex analyses into meaningful insights using data visualization and presentation tools
Ability to manipulate and analyze complex structured and unstructured data from multiple real-world evidence sources
Ability to work under pressure with a high level of autonomy/leadership on research projects
Ability to collaborate with multiple partners in a matrixed environment
Knowledge of the external regulatory environment for real-world evidence
Awareness of scientific developments in epidemiology, medicine, and technology, including artificial intelligence

Benefits

Comp & perks

Flexible workplace culture supporting work-life harmony
Reasonable adjustments and disability inclusion support
Equal employment opportunities
Patient-centric, values-driven workplace culture