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The Director of Biostatistics will provide scientific leadership and technical support for Pfizer's clinical and non-clinical projects, focusing on complex study designs, data analyses, and the development of specialized software. The role emphasizes collaboration across various therapeutic areas, training, methodological research, and external scientific collaborations to enhance statistical methodologies for drug development.

As a Director of Biostatistics at Pfizer, you will provide scientific leadership, assist with complex study designs, and collaborate with various teams on clinical and non-clinical projects. Your role will involve the development and implementation of statistical methodologies, ensuring adherence to regulatory guidelines, and fostering collaborations across various domains to advance drug development.

The Director of Biostatistics will provide scientific leadership and support for clinical and non-clinical projects at Pfizer, focusing on statistical research, study design, data analysis, and regulatory strategies. Responsibilities include collaboration with various teams, implementation of advanced methodologies, and external engagement with stakeholders in academia and industry.

As an Associate Director in Biostatistics, you will provide scientific consultancy and technical support to Pfizer's clinical and non-clinical projects, develop statistical methodologies, and engage in complex data analyses. Collaborating with various teams, the role emphasizes innovation in drug development and internal knowledge dissemination.

The Associate Director of Biostatistics will provide consultancy and technical support for global projects, focusing on statistical design and data analysis. They will collaborate with teams, develop software, advance statistical methodologies, and influence practices both internally and externally. Responsibilities include statistical advice, methodology development, and consultation for clinical and regulatory decisions.

The Associate Director of Biostatistics will provide scientific consultancy and technical support for global clinical and non-clinical projects, focusing on advanced study designs and data analyses. Responsibilities include collaboration with various teams, supporting innovation in statistical methodologies, and providing statistical advice for complex problems related to drug and vaccine development.

The Associate Director, Medical Monitor for Vaccine Research and Development oversees clinical trials, provides medical expertise, designs development strategies, ensures safety throughout studies, and collaborates with various teams to ensure compliance and quality data. Key responsibilities include protocol design, safety monitoring, and effective communication of safety information across sites.