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9 дней назад

Associate Director Statistical Programming (SAS)

176 100 - 287 300$
Формат работы
hybrid/onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Director Statistical Programming (SAS): Leading statistical programming activities for clinical development programs with an accent on advanced SAS programming, therapeutic-area support, and high-quality deliverables across internal and outsourced work. Focus on setting programming standards, managing interdisciplinary teams, guiding regulatory submissions, and mentoring direct reports.

Location: Warren, New Jersey, United States; onsite/hybrid work model

Salary: $176,100–$287,300 annually

Company

hirify.global is a biotechnology company that develops medicines for serious diseases and advances clinical programs across multiple therapeutic areas.

What you will do

  • Lead and manage a statistical programming group delivering work through internal teams and external service providers.
  • Define programming standards, applications, processes, and training for the assigned therapeutic area.
  • Partner with study and project teams to clarify requirements and guide programmers through execution.
  • Represent Statistical Programming with cross-functional partners to align specifications and computing needs.
  • Set goals, manage performance, mentor direct reports, and support hiring through candidate screening and interviews.
  • Drive department goals and subject-matter-expert initiatives while ensuring timely, high-quality deliverables.

Requirements

  • Master’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline.
  • 10+ years of clinical programming experience.
  • Advanced SAS programming skills, including Base, Stat, Macro, and Graph, in a clinical data environment.
  • Experience managing projects, people, and external service providers across global interdisciplinary teams.
  • Expertise in one or more therapeutic areas and strong knowledge of pharmaceutical clinical development and regulatory submissions.
  • Ability to work in the onsite/hybrid model in Warren, New Jersey.

Nice to have

  • SAS certification.
  • Leadership experience in hiring, developing, and evaluating junior staff and contractors.

Culture & Benefits

  • Science-driven environment focused on developing life-changing medicines.
  • Collaborative work with study teams, project teams, programming leadership, and cross-functional stakeholders.
  • Comprehensive rewards package that may include bonuses, equity, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
  • Inclusive workplace with reasonable accommodation available during the recruitment process where required.

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