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AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Senior Manager, Statistical programming

Req ID 2208255 Category Research and Development Division AbbVie
  • Supervise statistical programming group ; accountable for review and validation of all programmed results ;monitor and quantify efficiency' accuracy, and timeliness of group ; recruit, train, and orient all new hires;review project timelines and plans; accountable for development (technical and interpersonal skills ) of individual within the group; review project time lines and plans; provide headcount forecast for projects.
  • Manage all the programmers in the statistical programming department.
  • Ensure technology updates occur as needed
  • Guide programmers when they need assistance in programming.
  • Train and teach efficient programming techniques to programmers.
  • Provide programming support to analyze clinical data and generate reports and graphs on all AbbVie drugs in the clinical phase.
  • Hire consultant programmers to meet short -term needs of additional programming resources.
  • Ensure expenses for consultant programmers do not exceed the budget limitations.
  • Works with Director of Statistical Computing to establish and ensure adherence with programming and output standards and utilization of systems and processes to maximize efficiency of the statistical programming function
  • B.S., M.S. or Ph.D. in statistics, computer science, mathematics or a related field, required
  • 7 years of experience in the pharmaceutical industry generating analysis , reports and graphs for individual studies and ISS, ISE, NDA submissions to FDA.
  • Minimum of 2 years of supervisory experience
  • Excellent programming skills especially in SAS
  • Excellent problem solving, leadership, communication and interpersonal skills.Working knowledge of current regulatory requirements and guidancedemonstrated ability to debug SAS programs and assist programmers
Significant Work Activities: N/A
Travel: No
Job Type: Experienced
Schedule: Full-time

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