Pipeline - Manager, Statistical Programming (Remote)

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 Twitter, Facebook, Instagram, YouTube and LinkedIn.

Job Description

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. Therapeutic Areas include Immunology, Oncology, Neuroscience, Eye Care, Aesthetics, and other Specialties.

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

Qualifications

• 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.

Key Stakeholders:

• Statisticians • Data Scientists • Medical Writers • Regulatory Publishers

Additional Information

Applicable only to applicants