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Manager - Statistical Programming (Hybrid)

AbbVie
June 30, 2026
Remote friendly (Florham Park, NJ)
United States
$109,500 - $208,500 USD yearly
Clinical Research and Development
The Manager of Statistical Programming is responsible for leading statistical programming activities for the Neuroscience group and effectively interfacing with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Clinical Operations.

Responsibilities:
- Lead statistical programming activities for a compound/indication or therapeutic area in early development.
- Lead a team of statistical programmers and manage resource planning for assigned staff.
- Ensure timely deliverables, quality processes, and consistency within projects.
- Develop and oversee SAS programs for ADaM data set creation following CDISC standards.
- Develop and oversee SAS programs for Tables, Listings, and Figures.
- Ensure consistency of ADaM data sets for individual studies and integrated data.
- Create documentation for regulatory filings (reviewer guides, data definition documents).
- Lead development of standard SAS Macros and participate in SOP development.
- Provide oversight and mentoring to Statistical Programmers and analysts.

Qualifications:
- Bachelors in Statistics or Mathematics.
- 10+ years relevant experience (or 8+ with a Masters).
- Experience leading a team/project of statistical programmers.
- SAS programming experience for drug development.
- In-depth understanding of CDISC standards.
- Experience with ADaM development and TLF generation.

Preferred:
- Experience with regulatory filings.

Required skills:
- Clear oral and written communication.
- Represent Statistical Programming Organization in cross-functional teams.
- Accurately estimate effort for programming activities.

Benefits (as stated):
- Paid time off; medical/dental/vision insurance; 401(k); eligible for long-term incentive programs.