Associate Director - Statistics, Specialty TA (Hybrid)

Added
10 days ago
Type
Full time
Salary
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Related skills

statistics sap biostatistics clinical trials regulatory submissions
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๐Ÿ“‹ Description

  • Provide expertise/lead regulatory submission and product life-cycle management strategy planning
  • Represent function/department on project team(s) to provide statistical input to compound/drug
  • Demonstrate extensive understanding of statistical concepts and methodology. Propose novel
  • Train and mentor staff on statistical methodology and operations. May supervise contract
  • Develop strategy for data presentation and inference. Ensure appropriate interpretation of
  • Act as the liaison for statistical issues on AbbVie collaborative studies with CROs, academic

๐ŸŽฏ Requirements

  • MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics
  • Strong leadership skills and experience in working/managing cross-cultural or oversea teams
  • Pharmaceutical or related industry knowledge required, including proven experience and
  • PhD preferred
  • Submission experience preferred
  • Technical competence and excellent communication skills, both oral and written

๐ŸŽ Benefits

  • Comprehensive package of benefits including paid time off (vacation, holidays, sick)
  • Eligible to participate in long-term incentive programs
  • Bonuses, commission, and incentives are earned, vested, and determinable
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