Senior Statistical Analyst

The Senior Statistical Analyst/Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics Data Sciences Medical Writing Regulatory Publishing and Clinical Operations.

• Leads the statistical programming activities for projects with lower complexity.
• Leads the statistical programming activities for studies.
• Develop SAS programs for the creation of ADaM data sets following CDISC standards.
• Develop SAS programs for the creation of Tables Listings and Figures.
• Validation of ADaM data sets Tables Listings and Figures.
• Create specifications for the structure of ADaM data sets for individual studies and integrated data.
• Create 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 and Statistical Analysts.

Qualifications :

The position will be hired based on the qualifications below: 

Senior Statistical Analyst:

• MS in Statistics Computer Science or a related field with 6 years of relevant experience. OR BS in Statistics Computer Science or a related field with 8 years of relevant experience.
• In depth understanding of SAS programming concepts and techniques related to drug development.
• Fundamental understanding of CDISC Standards.
• Fundamental understanding of the drug development process including experience with regulatory filings.
• Ability to communicate clearly both oral and written.
• Ability to accurately estimate effort required for study related programming activities.

Statistical Analyst:

• MS in Statistics Computer Science or a related field with 3 years of relevant experience. OR BS in Statistics Computer Science or a related field with 5 years of relevant experience.
• Demonstrated practical understanding of SAS programming concepts and techniques related to drug development.
• Basic understanding of CDISC Standards.
• Basic understanding of the drug development process.
• Ability to communicate clearly both oral and written.

This a remote opportunity and can be hired anywhere in the US. 

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. 

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 :

Yes