AbbVie
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Senior Manager, Statistical Programming
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AbbVie
Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at
www.abbvie.com . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.
Job Description Purpose
The Senior Manager of Statistical Programming is a leadership role managing a team of statistical programmers in pharmaceutical research and development. Responsible for leading statistical programming activities for one or more compounds, indications, or therapeutic areas, interfacing effectively with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Development Operations.
Responsibilities
Lead statistical programming activities for assigned compounds or therapeutic areas.
Manage a team of statistical programmers and resource planning.
Ensure timely deliverables, adherence to quality processes, and consistency across projects.
Develop and oversee SAS programs for ADaM data sets following CDISC standards.
Create SAS programs for Tables, Listings, and Figures.
Ensure consistency of ADaM data sets for studies and integrated data.
Prepare documentation for regulatory filings, including review guides and data definition documents.
Lead development of standard SAS Macros and SOPs.
Manage, mentor, and develop career plans for staff.
Participate in recruitment and selection of new staff.
Qualifications
MS in Statistics, Computer Science, or related field with 9+ years of relevant experience, or BS with 11+ years.
Minimum of 2 years leading a team of statistical programmers.
Deep understanding of SAS programming and drug development processes.
Knowledge of CDISC Standards.
Understanding of regulatory filings and drug development.
Excellent communication skills.
Ability to estimate effort for programming activities.
Additional Information Position requires on-site presence 3 days/week. Compensation range is based on geographic location and experience. Benefits include health insurance, 401(k), and participation in incentive programs. AbbVie is an equal opportunity employer committed to diversity and inclusion.
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Senior Manager, Statistical Programming
role at
AbbVie
Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at
www.abbvie.com . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.
Job Description Purpose
The Senior Manager of Statistical Programming is a leadership role managing a team of statistical programmers in pharmaceutical research and development. Responsible for leading statistical programming activities for one or more compounds, indications, or therapeutic areas, interfacing effectively with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Development Operations.
Responsibilities
Lead statistical programming activities for assigned compounds or therapeutic areas.
Manage a team of statistical programmers and resource planning.
Ensure timely deliverables, adherence to quality processes, and consistency across projects.
Develop and oversee SAS programs for ADaM data sets following CDISC standards.
Create SAS programs for Tables, Listings, and Figures.
Ensure consistency of ADaM data sets for studies and integrated data.
Prepare documentation for regulatory filings, including review guides and data definition documents.
Lead development of standard SAS Macros and SOPs.
Manage, mentor, and develop career plans for staff.
Participate in recruitment and selection of new staff.
Qualifications
MS in Statistics, Computer Science, or related field with 9+ years of relevant experience, or BS with 11+ years.
Minimum of 2 years leading a team of statistical programmers.
Deep understanding of SAS programming and drug development processes.
Knowledge of CDISC Standards.
Understanding of regulatory filings and drug development.
Excellent communication skills.
Ability to estimate effort for programming activities.
Additional Information Position requires on-site presence 3 days/week. Compensation range is based on geographic location and experience. Benefits include health insurance, 401(k), and participation in incentive programs. AbbVie is an equal opportunity employer committed to diversity and inclusion.
#J-18808-Ljbffr