Director, Metrics & Reporting Lead, Central Services, Data Monitoring & Management
As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Metrics and Reporting Lead is responsible for ensuring that reporting that illustrates portfolio performance are generated and communicated across DMM, Statistical Programming and Analysis (SPA) and Medical Writing. The role will ensure that clinical trial quality reporting is available to support Quality Assurance activities. The role may also support reporting activities across Pfizer.
Delivers data analysis reporting operational services to GBDM and other groups within Pfizer
Serves as lead subject matter expert for advanced metrics solutions related to data analysis reporting/programming. Understands and anticipates business priorities, products, and information needs
Supporting reporting activities for Operational and Quality Steering Committee (OQSC) and Clinical Trial Process Quality (CTPQ) measures
Leads performance reporting discussions both internally and externally with internal stakeholders and service providers
Targets reporting to address key performance and delivery questions which includes root cause assessment and generation of high level messages that support reporting output
Collaborates with other Pfizer metrics SMEs to support Pfizer initiatives and remain aligned with other Pfizer metrics and reporting activities
Supports business reporting solutions for GBDM inclusive of presenting and communicating results that improve performance
Bachelor's degree required in a statistical or scientific field. Advanced degree preferred.
Experience and or training specific to statistical programming and statistics reporting software (e.g. SAS) and visualization tools (e.g. Spotfire)
At least 10 years relevant experience in a pharmaceutical, biotech, CRO or Regulatory Agency with at least 5 years being related to reporting and analysis solutions with an emphasis on Programming and Data Management.
Thorough understanding of regulatory requirements and relevant data standards
Strong leadership, influencing, negotiation, and management skills
Data Management and clinical trials expertise with a thorough understanding of the processes associated with clinical drug development and data analysis operations required for the reporting of clinical trials and global regulatory submissions.
Thorough understanding of regulatory requirements and relevant data standards. CDISC knowledge and experience are preferable.
Strong communication (written and oral), leadership, decision-making, influencing, negotiation, and project management skills
Sound knowledge and experience working across international boundaries and cultures.
Primarily an office-based position involving sitting in front of a computer for large periods of work time, making presentations, etc.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Ability to travel approximately 5 to 10%.
EEO & Employment Eligibility
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