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De missie van AbbVie is het ontdekken en leveren van innovatieve geneesmiddelen die vandaag een oplossing bieden voor ernstige gezondheidsproblemen en de medische uitdagingen van morgen aanpakken. We streven ernaar om een grote impact te hebben op het leven van mensen in verschillende belangrijke therapeutische domeinen: immunologie, oncologie, neurowetenschappen, oogzorg, virologie, vrouwengezondheid en gastro-enterologie, naast producten en diensten uit de portefeuille van Allergan Aesthetics. Bezoek www.abbvie.com voor meer informatie over AbbVie. Volg @abbvie op Twitter, Facebook, Instagram, YouTube en LinkedIn.
Senior Manager, Statistical Programming (Remote)
Waukegan, Illinois Job ID 2116527 Categorie Research and Development Afdeling 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
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