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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 www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Senior Manager, Statistical Programming (Remote)

Lake County, Illinois Req ID 2116527 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
Qualifications:
  • 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: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel: No
Job Type: Experienced
Schedule: Full-time
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