Director

• Works closely with CDIS and SDSA department roles and cross-functional study team members to create reporting and analytics solutions that support the quality and timely delivery of data management reports and visualizations required per standard and study specific data review plans
• Delivers data analysis reporting operational services to CD&O and other groups within Pfizer
• Supports business reporting solutions for CD&O inclusive of presenting and communicating results that improve performance
• Creates any needed documentation for reports throughout the lifespan of the study and or asset for all DMRA deliverables and ensures proper filing in the Trial Master File filings when appropriate
• Complies with applicable SOPs and work practices
• Serves on the data standards board as needed and leads as needed implementation and where needed development of data management reporting standards
• Serve as a technical resource to the study teams for data visualization and reporting tools
• Ensure operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan, in collaboration with the Clinical Data Scientist, ensure operational excellence across all CDIS and SDSA deliverables
• Directly supports knowledge development of others on reporting and analytics tools that support the accuracy and integrity of study data
• Identifies existing process/product improvements
• Develops innovative, advanced new concepts that improve processes / products across own and related disciplines
• Takes appropriate risks to achieve desired results
• Recognizes development needs and identifies/creates development opportunities within own team
• Develops a talent base and anticipates development needs within the area of responsibility

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