AbbVie has acquired Allergan, and we’ve moved sites!

As one company, we have brought together over 30 brands and leadership positions, expanding and diversifying our product portfolio. Join us in making a remarkable impact on people’s lives around the world. Visit careers.abbvie.com to explore our career opportunities. If you are a current AbbVie or legacy Allergan employee, please visit your intranet site to apply internally.


To apply internally on the AbbVie intranet site please go to myabbvie.abbvienet.com. Next, hover over resources and then select Human Resources. After that, you will select “Global Job Board.” You are now viewing jobs on our internal site.


To apply internally on the Allergan intranet site please go to https://allergan.sharepoint.com/sites/GEP. Select the “AbbVie Jobs” tile under the Tools section.

About AbbVie

AbbVie (NYSE:ABBV) is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world.  For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook or LinkedIn.​

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Sr. Principal Statistical Analyst/Associate Director, Statistical Programming

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Research & Development
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2002471 Requisition #
Thanks for your interest in the Sr. Principal Statistical Analyst/Associate Director, Statistical Programming position. Unfortunately this position has been closed but you can search our 0 open jobs by clicking here.

 

  • High degree of technical competence and strong communication ability, both oral and written.
  • Highly competent in SAS programming and Macro development.

  • Pharmaceutical experience with clinical trials, including familiarity with expectations of regulatory agencies, especially FDA and EMEA. NDA/BLA or other regulatory filing experience, including ISS or ISE experience.

  • Thorough understanding of ICH Guidelines and relevant regulatory requirements.

  • Understand CDISC standards and applicability to clinical database design/capture and reporting.

  • Knowledge in integrating SAS with other leading technologies such as Extensible Markup Language (XML), Microsoft Office, etc. to support electronic submissions.

  • Knowledge of Pinnacle 21.

  • Understand about reviewer’s guides and Define.xml.

    Education and Experience:

  • MS in Statistics, Computer Science, Bioinformatics, Biostatistics, or a related field with 10+ years of relevant experience; OR BS in Statistics, Computer Science or a related field with 12+ years of relevant experience.

 

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At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients.  As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.

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