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24 часа назад

Senior Manager, Statistical Programming (SAS)

150 500 - 245 500$
Формат работы
hybrid/onsite
Тип работы
fulltime
Грейд
senior
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
Senior Manager, Statistical Programming (SAS): Leading statistical programming deliverables across clinical studies through regulatory approval and product launch with an accent on advanced SAS programming, clinical trial data, and regulatory submissions. Focus on coordinating global cross-functional teams, preparing submission-ready deliverables, and mentoring programmers while managing multiple studies and priorities.

Location: Warren, New Jersey or Cambridge, Massachusetts; hybrid-onsite

Salary: $150,500–$245,500 annually

Company

hirify.global is a biotechnology company that discovers, develops, and commercializes medicines for serious diseases.

What you will do

  • Lead statistical programming support across multiple clinical studies and therapeutic areas.
  • Coordinate programming documentation and specifications according to established standards.
  • Deliver submission-ready programming outputs for global regulatory authority filings.
  • Communicate with study and project teams to clarify requirements and guide programmers.
  • Serve as a statistical programming subject matter expert and contribute to department strategy.
  • Set goals, coach, and mentor direct reports, while supporting hiring through candidate screening and interviews.

Requirements

  • Advanced SAS programming expertise in a clinical data environment.
  • Strong understanding of clinical trial principles, statistical concepts, and regulatory submission requirements.
  • Experience leading global, cross-functional teams and managing multiple concurrent projects.
  • Mentoring or coaching experience with junior programmers.
  • BS or MS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline.
  • 10+ years of programming experience, or 12+ years with a BS, preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries, including project and people management experience.

Nice to have

  • Knowledge of R or Python.

Culture & Benefits

  • Science-driven work focused on developing medicines for serious diseases.
  • Inclusive workplace and equal opportunity employment.
  • Benefits may include annual bonuses, equity awards, retirement benefits, 401(k) matching, health and wellness programs, insurance, paid time off, and family support.
  • Background checks may be conducted to verify identity, right to work, and educational qualifications.

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