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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 of Biostatistics is responsible for designing, analyzing, and interpreting clinical trials while ensuring compliance with regulatory standards. Key tasks include providing statistical expertise for clinical development projects, leading statistical analyses, communicating results, and collaborating with cross-functional teams. This role requires strong leadership in statistical methodology and the ability to influence regulatory practices.

The Associate Director of Biostatistics will design, analyze, and interpret clinical trials and observational studies while ensuring compliance with regulatory requirements and Pfizer standards. They will provide statistical expertise in study design, analyses, and communicating results, working collaboratively with cross-functional teams for various clinical development projects and regulatory submissions.

The Associate Director of Biostatistics will design and analyze clinical trials, provide statistical expertise for clinical development and regulatory submissions, and ensure compliance with Pfizer standards. Responsibilities include planning statistical analyses, communicating findings, and leading collaborations with clinical teams. The role requires statistical leadership across projects and involvement in research related to statistical methodology.

The Associate Director of Biostatistics is responsible for designing and analyzing clinical trials and observational studies, providing statistical expertise for regulatory submissions, and leading statistical initiatives across projects. This role involves collaboration with various teams to ensure compliance with regulatory standards and the delivery of high-quality statistical results for scientific reports and publications.

The Associate Director of Biostatistics is responsible for designing, analyzing, and interpreting clinical trials and observational studies while ensuring compliance with regulatory requirements. This role involves providing statistical expertise for clinical development, regulatory submissions, and scientific reports, as well as fostering collaborations across clinical teams and leading statistical activities in study planning and execution.

The Associate Director, Biostatistics is responsible for designing, analyzing, and interpreting clinical trials and observational studies. They provide statistical expertise on clinical development projects and regulatory submissions, ensuring compliance with regulatory standards and internal guidelines. Responsibilities include statistical analysis planning, communication of results, and collaboration with internal and external stakeholders, while maintaining high-quality deliverables in a timely manner.