North Chicago, IL
20 hours ago
Statistical Programmer (Data & Statistical Sciences (DSS))

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

Key Responsibilities

Interface with DSS. Serve as an integral project team member in R & D of new pharmaceutical products.Analyze & report clinical trial data under direction of Senior Statistical Analyst.Provide SAS programming support for clinical trials.Develop SAS programs for creation of Analyst Data Models (ADaM), data sets following CDISC standards for either production/validation with creating specifications for structure of ADaM data sets for individual studies. Develop SAS programs for creation of Tables, Listings & Figures for either production/validation, also responsible for accuracy of SAS programs by reviewing output, code, & log files.
Qualifications

Education & Experience

Must possess a MS in Statistics, Biostatistics, Computer Science, or a related field and 6 months of relevant statistical programming experience, or alternatively, would accept BS in Statistics, Biostatistics, Computer Science or related field and 2 years of relevant statistical programming experience.

With either combination of education or work experience, must have  6 months of related experience in the following:

providing SAS programming support for pharmaceutical industry clinical trials;coding SAS programs using SAS base;utilizing SAS tools SAS/MACROS, SAS/SQL, SAS/GRAPH, & SAS/STAT;developing ADaM datasets in compliance with CDISC standards & developing Tables, Listings, & figures;  creating documentation for regulatory filings including reviewers’ guides & data definition documents, &complying with FDA & EMEA regulatory agencies/ICH guidelines & relevant regulatory requirements.

Experience may be gained concurrently. Any suitable combination of education, training or experience is acceptable.


Additional Information

100% telecommuting permitted

Salary Range: $102,523 - $118,500 per year.

Apply online at https://careers.abbvie.com/en. Refer to Req ID: REF36010H

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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 short-term and long-term incentive programs.

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html 

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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