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/Biostatistics or related field with 8+ years' experience or PhD in Statistics/Biostatistics or related field with 5+ years' experience in clinical trials Understanding of broad statistical theory and its
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statistics community at Pfizer through collaborations, scholarship, presentations, and learnings across divisions. BASIC QUALIFICATIONS Advanced degree in statistics, biostatistics, or related field. (PhD
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throughout clinical drug development in collaboration with pharmacometrics and statistics (as relevant). Provides recommendations for clinical doses and dosing algorithms (including drug interaction advice
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statistics, biostatistics, or related field required. PhD preferred. 15+ years of experience in drug development 5-10 years of experience in vaccine development At least 5 years of managerial experience in
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+ year of experience, or PhD and 0-3 years of experience Degree in chemistry, biochemistry, chemical engineering, or related field Direct experience with antibodies, proteins, and/or bioconjugation Good
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functional genomic screening to drive team success. Qualifications Must Have PhD or equivalent in cell biology and functional genomics. Experience developing and applying diverse functional assay readouts
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approaches. You will partner with key stakeholders and colleagues in Clinical Pharmacology, Quantitative Systems Pharmacology, Statistics, Translational Modeling and Simulation, and other Research and
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of experience OR Masters Degree with 6+ years of experience OR PhD with 2+ years of experience • Degree preferably in engineering, economics, statistics, computer science, or related quantitative field
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on deliverables throughout the process Provide input for the design of the Statistical Analysis Plan (SAP) and the clinical data output Responsible for review of patient level data across a study and for
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8 years of experience OR a Bachelor's degree with at least 5 years of experience OR Master's Degree with more than 3 years of experience, OR a PhD with 0+ years of experience. Excellent project