Senior Manager Statistical Programming

Purpose

The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics Data Sciences Medical Writing Regulatory Publishing and Development Operations.

Responsibilities

• Manages a team of statistical programmers and the resource planning for their assigned projects.
• 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 the development of standard operating procedures.
• Manages mentors and creates career development plans for assigned staff.
• Participates in the recruitment and selection of new staff.

Qualifications :

*This position will be required to sit onsite 3 days / week*

Qualifications

• MS in Statistics Computer Science or a related field with 9 years of relevant experience. OR BS in Statistics Computer Science or a related field with 11 years of relevant experience.
• Minimum of 2 years experience leading a team of statistical programmers.
• Indepth understanding of SAS programming concepts and techniques related to drug development.
• Indepth understanding of CDISC Standards.
• Indepth 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 

Directors of Statistics
Data Scientists
Medical Writers
Regulatory Publishers
Clinical Project Managers

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: 

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.

• We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.

• This job is eligible to participate in our shortterm incentive programs. 

• This job is eligible to participate in our longterm incentive programs

Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law. 

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. 

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Work :

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