Summary
Join AbbVie as a Manager of Statistical Programming, a strategic role guiding a team in pharmaceutical product R&D. Lead statistical programming activities for a compound/indication or therapeutic area in early development. Manage a team of statistical programmers, ensuring timely deliverables and adherence to quality processes. Develop and oversee SAS programs for ADaM datasets and TFLs, following CDISC standards. Create documentation for regulatory filings and lead the development of standard SAS macros and SOPs. Provide oversight and mentoring to statistical programmers and analysts. This remote US-based position requires strong SAS programming, CDISC, and drug development knowledge.
Requirements
- MS in Statistics, Computer Science or a related field with 8+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 10+ years of relevant experience
- Previous experience leading a team of statistical programmers
- In-depth understanding of SAS programming concepts and techniques related to drug development
- In-depth understanding of CDISC Standards
- In-depth understanding of the drug development process, including experience with regulatory filings
- Ability to communicate clearly both oral and written
- Ability to effectively represent the Statistical Programming Organization in cross functional teams
- Ability to accurately estimate effort required for project related programming activities
Responsibilities
- Leads the statistical programming activities for a compound/indication or therapeutic area in early development
- Leads a team of statistical programmers and manages the resource planning for assigned staff
- Ensures timely deliverables, that all quality processes are followed and consistency within the projects
- Develops and oversees the development of SAS programs for the creation of ADaM data sets following CDISC standards
- Develops and oversees the development of SAS programs for the creation of Tables, Listings and Figures
- Ensures consistency of ADaM data sets for individual studies and integrated data
- Creates documentation for regulatory filings including reviewers guides and data definition documents
- Leads the development of standard SAS Macros and participates in the development of standard operating procedures
- Provides oversight and mentoring of assigned Statistical Programmers, Statistical Analysts and Senior Statistical Analysts
Benefits
- Paid time off (vacation, holidays, sick)
- Medical/dental/vision insurance
- 401(k)
- Short-term incentive programs
- Long-term incentive programs
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