Manager, Statistical Programming

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. You will manage resources, ensure timely deliverables, and develop SAS programs adhering to CDISC standards. Collaborate with various teams, including Statistics, Data Sciences, and Medical Writing. This remote US-based position requires an MS in a related field with 8+ years of experience or a BS with 10+ years, along with proven team leadership in statistical programming and a deep understanding of SAS, CDISC, and drug development.

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

• Lead the statistical programming activities for a compound/indication or therapeutic area in early development
• Lead a team of statistical programmers and manage the resource planning for assigned staff
• Ensure timely deliverables, that all quality processes are followed and consistency within the projects
• Develop and oversee the development of SAS programs for the creation of ADaM data sets following CDISC standards
• Develop and oversee the development of SAS programs for the creation of Tables, Listings and Figures
• Ensure consistency of ADaM data sets for individual studies and integrated data
• Create documentation for regulatory filings including reviewers guides and data definition documents
• Lead the development of standard SAS Macros and participate in the development of standard operating procedures
• Provide oversight and mentoring of assigned Statistical Programmers, Statistical Analysts and Senior Statistical Analysts

Preferred Qualifications

This is a remote opportunity that can be hired anywhere in the US

Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Short-term incentive programs
• Long-term incentive programs