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6 часов назад

Principal Biostatistician (Clinical Trials)

130 000 - 220 000$
Формат работы
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

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TL;DR
Principal Biostatistician (Clinical Trials): Analyzing clinical trial datasets and evidence across a biopharmaceutical pipeline with an accent on signal detection, statistical modeling, and evidence synthesis. Focus on building mixed-effects, longitudinal, Bayesian, subgroup, and sensitivity analyses, pressure-testing clinical assumptions, and translating complex findings into pipeline and commercialization decisions.

Location: New York, NY, United States

Salary: $130,000–$220,000 per year at commencement of employment; final compensation may vary.

Company

hirify.global is a biopharmaceutical company developing and commercializing medicines through a portfolio of specialized subsidiaries and technology ventures.

What you will do

  • Analyze ongoing and completed clinical trial datasets to identify efficacy signals, safety patterns, and subgroup effects.
  • Build statistical analyses using mixed-effects, longitudinal, Bayesian, subgroup, and sensitivity-analysis frameworks.
  • Monitor emerging safety signals and unexpected findings, contextualizing results for leadership.
  • Pressure-test endpoints, statistical analysis plans, and clinical assumptions across pipeline assets.
  • Execute focused analytical sprints addressing high-priority questions from Roivant and Vant leadership.
  • Synthesize trial, literature, registry, claims, laboratory, genomics, and proprietary data into evidence narratives.

Requirements

  • Advanced degree in biostatistics, statistics, epidemiology, or a closely related quantitative field.
  • Hands-on experience working with patient-level clinical trial datasets.
  • Strong knowledge of mixed-effects models, longitudinal and repeated-measures analyses, Bayesian methods, multiplicity adjustment, and sensitivity analyses.
  • Familiarity with clinical trial design and regulatory statistical frameworks, including ICH E9, estimands, and SAP development.
  • Demonstrated ability to translate rigorous analysis into business and clinical decisions.
  • Ability to explain complex statistical findings clearly to non-technical and CEO-level stakeholders.

Culture & Benefits

  • Full-time, at-will employment.
  • Meaningful equity participation.
  • Comprehensive company-sponsored benefits package.
  • Direct exposure to senior leadership and ownership of high-stakes clinical evidence decisions.
  • Opportunity to support commercialization across multiple biopharmaceutical assets.

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