Associate Director, Statistics - Immunology (Hybrid)

Added
1 day ago
Type
Full time
Salary
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Related skills

statistics biostatistics patient safety regulatory submissions clinical development

πŸ“‹ Description

  • Provide expertise/lead regulatory submission and product life-cycle management strategy planning
  • Provide statistical leadership for design, analysis and reporting for clinical or other scientific
  • Independently develop protocols and statistical analysis plans (or product safety analysis
  • Represent function/department on project team(s) to provide statistical input to compound/drug
  • Partner with other functions (Clinical, Regulatory, Patient Safety, or GMA) to create development
  • Demonstrate extensive understanding of statistical concepts and methodology; propose novel

🎯 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 overseas teams.
  • Pharmaceutical knowledge required, including experience and understanding of drug development and
  • Preferred: Experience with late-stage clinical trials and/or submissions.
  • Preferred: Experience with immunology clinical trials.
  • High degree of technical competence and excellent communication skills, both oral and written.

🎁 Benefits

  • Comprehensive package of benefits including paid time off (vacation, holidays, sick)
  • Medical/dental/vision insurance and 401(k) to eligible employees
  • Eligibility to participate in long-term incentive programs
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