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1 день назад

Senior Director, Biostatistics - Immunology & Inflammation (Biotechnology)

242 000 - 403 300$
Формат работы
hybrid
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
Senior Director, Biostatistics - Immunology & Inflammation (Biotechnology): Leading strategic and operational biostatistics activities for immunology and inflammation clinical development programs with an accent on statistical support, regulatory submissions, and departmental growth. Focus on designing clinical studies, reviewing statistical analyses and reports, mentoring teams, and influencing cross-functional and senior-management decisions.

Location: Tarrytown, NY; Cambridge, MA; or Warren, NJ, United States. Four days per week onsite; up to 25% travel may be required.

Salary: $242,000–$403,300 annually

Company

Science-driven biotechnology organization developing medicines for people with serious diseases.

What you will do

  • Lead strategic and operational biostatistics activities for the immunology and inflammation therapeutic area.
  • Define departmental goals, allocate resources, and plan project timelines across the product pipeline.
  • Provide statistical leadership for clinical development plans, study design, operational activities, and key project decisions.
  • Oversee statistical reporting and review SAPs, analysis presentations, clinical study reports, and integrated summaries.
  • Represent biostatistics in regulatory meetings and cross-functional committees, including interactions with senior leadership.
  • Recruit, mentor, develop, and retain biostatistics staff while promoting quality, teamwork, and compliance.

Requirements

  • Ph.D. in statistics or a related discipline with 10+ years of biotechnology, pharmaceutical, or healthcare industry experience, or an M.S. with 15+ years of experience.
  • Six or more years of successful project and people management experience, including significant interaction with the FDA and EMEA.
  • Advanced knowledge of statistical concepts and techniques, pharmaceutical clinical development, regulatory submissions, and statistical practice.
  • Experience across multiple therapeutic areas and active research interests related to clinical trials.
  • Strong leadership, project management, teamwork, communication, presentation, administrative, and influencing skills.
  • Proven ability to lead major process and technology initiatives across multiple functional groups and adapt methods to complex problems.

Culture & Benefits

  • Inclusive workplace focused on science, innovation, and meaningful patient impact.
  • Competitive total rewards package that may include annual bonuses, equity awards, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
  • Collaborative onsite working environment with opportunities to work closely with medical study directors and cross-functional teams.

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