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Conduct statistical tasks related to clinical trials and approval submission documents for a vaccine project, including creating statistical analysis plans and providing statistical advice. Programming support as needed and collaborating with global teams.

The Senior Statistical Data Scientist will program statistical deliverables, collaborate with study teams, and ensure compliance with Pfizer standards, focusing on SAS, R, or Python. They will also engage in self-learning and contribute to SDSA initiatives.

The role involves programming deliverables for statistical projects, mentoring team members, ensuring quality standards, and collaborating across teams to meet project goals.

The role involves managing regulatory activities for post-approval CMC changes, ensuring stable product supply, and providing regulatory information to support development processes.

Intern will support and develop features in a web project, applying data cleansing and implementing visualizations for customers.

The Data Manager oversees data management for clinical trials, ensuring data quality, query management, and compliance with operational standards within the Clinical Data Sciences group.

The Senior Manager leads BI dashboard design and development, ensuring data integrity and governance while collaborating across teams for analytics solutions that support commercial decision-making.

The Senior Associate executes performance reporting, validates data, ensures quality control, and collaborates with analytics teams to meet reporting demands.

The Senior Data Scientist will lead care gap analyses and HCP segmentation projects, supporting strategic planning and mentorship within the team while leveraging advanced analytical techniques.

Manage performance analytics and insights to support commercial strategies at Pfizer. Develop in-house data sets, analyze performance, and provide actionable recommendations to stakeholders. Collaborate with analytical teams to enhance reporting processes and tools.