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Manager, Statistical Programming (Remote)

  2025-11-02     BioSpace     all cities,AK  
Description:

Manager, Statistical Programming (Remote)

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The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly responsible for leading the statistical programming activities for a compound/indication or therapeutic area in early development. The Manager of Statistical Programming must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.

Responsibilities

  • Leads the statistical programming activities for a compound/indication or therapeutic area in early development.
  • Leads a team of statistical programmers and manages 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.

Qualifications
  • This is a remote opportunity that can be hired anywhere in the US.
  • 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.
  • Excellent oral and written communication skills.
  • Ability to effectively represent the Statistical Programming Organization in cross-functional teams.
  • Ability to accurately estimate effort required for project-related programming activities.

Additional Information
  • The compensation range described below is the range of possible base pay compensation at the time of posting. Individual compensation paid within this range will depend on factors including geographic location and may be modified in the future. Salary: $106,500 - $202,500
  • We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.
  • This job is eligible to participate in our long-term incentive programs.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

Seniority level

  • Mid-Senior level

Employment type
  • Full-time

Job function
  • Design, Art/Creative, and Information Technology

Industries
  • Internet News

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