Join to apply for the Clinical Statistician, Associate Director role at Pfizer 2 days ago Be among the first 25 applicants Join to apply for the Clinical Statistician, Associate Director role at Pfizer Job Summary This position provides statistical support for clinical and scientific projects led by the Rheumatology group within the Inflammation and Immunology & Specialty Care disease area at Pfizer Research and Development. The successful candidate will collaborate closely with cross-functional project and study teams, offering statistical expertise in designing clinical trials, developing protocols, writing statistical analysis plans, performing statistical analyses, interpreting and presenting results, writing/reviewing reports, and publishing manuscripts through co-authorship. The candidate may also provide support in regulatory submissions including responses to regulatory queries. Successful candidate will make contributions through quantitative and creative thinking as well as proactively staying in the front of the current development of statistical methodologies. Proficiency in at least one statistical programming language (R, SAS, or Python) is required. Job Summary This position provides statistical support for clinical and scientific projects led by the Rheumatology group within the Inflammation and Immunology & Specialty Care disease area at Pfizer Research and Development. The successful candidate will collaborate closely with cross-functional project and study teams, offering statistical expertise in designing clinical trials, developing protocols, writing statistical analysis plans, performing statistical analyses, interpreting and presenting results, writing/reviewing reports, and publishing manuscripts through co-authorship. The candidate may also provide support in regulatory submissions including responses to regulatory queries. Successful candidate will make contributions through quantitative and creative thinking as well as proactively staying in the front of the current development of statistical methodologies. Proficiency in at least one statistical programming language (R, SAS, or Python) is required. Job Responsibilities Provide scientifically rigorous statistical input into project development plans, regulatory submissions, interpretation of statistical results, study design, statistical analysis plans and scientific and commercialization projects. Be accountable for quality statistical deliverables according to study and submission timelines. Develop effective communication and collaborations with clinical teams, partner lines, and external organizations. Provide statistical input and leadership to cross-functional activities – collaborate with other statisticians, study managers, programmers – for assigned studies and regulatory submissions. Ensure that all study and project level statistical activities are conducted in compliance with relevant regulatory requirements and Pfizer standards. Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results, modeling and simulation in support of various activities, support for publications, scientific presentations, and support to product defense. Provide a strong statistical presence in regulatory and professional circles to influence content of regulatory guidelines and their interpretation in practice. Help maintain a strong statistics community at Pfizer through research collaborations, scholarship, presentations and learnings across divisions and locations. Qualifications / Skills
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