Назад
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8 дней назад

Senior Director, Biostatistics

250 000 - 300 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/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 (Biotechnology): Leading statistical planning, analysis, and interpretation across preclinical and clinical development programs with an accent on complex datasets, regulatory compliance, and biometrics infrastructure. Focus on designing advanced statistical approaches, overseeing CROs and biometrics vendors, supporting global regulatory submissions, and solving risks across cross-functional clinical teams.

Location: South San Francisco, United States; hybrid schedule with on-site work required at least three days per week

Salary: $250,000–$300,000 annually

Company

hirify.global is a clinical-stage biotechnology company developing genetically validated therapies for cardioendocrine diseases, including severe hypertriglyceridemia and acromegaly.

What you will do

  • Lead statistical planning, analysis, and interpretation across preclinical and clinical development programs.
  • Develop strategic and creative statistical approaches aligned with regulatory and industry standards.
  • Serve as the Biostatistics representative on clinical study teams and collaborate across functions.
  • Oversee CROs, biometrics vendors, consultants, statisticians, programmers, and data managers.
  • Support global regulatory strategy, submissions, interactions, publications, and communications.
  • Establish best practices for data handling, infrastructure, scientific interpretation, resourcing, and risk management.

Requirements

  • PhD and 10+ years of biostatistics experience in the biotechnology or pharmaceutical industry.
  • Expertise in applied statistics, including complex dataset design and analysis, multiple imputation, and longitudinal data analysis.
  • Proven experience leading teams and external vendors, including statisticians, programmers, and data managers.
  • In-depth knowledge of all phases of global drug development and regulatory submission processes.
  • Strong cross-functional communication, presentation, project management, attention to detail, and problem-solving skills.
  • Ability to work on-site in South San Francisco at least three days per week.

Nice to have

  • Experience in cardiovascular, metabolic, or rare diseases.
  • Experience supporting large, long-term studies and clinical development plans.

Culture & Benefits

  • Collaborative, hands-on environment with direct contributions across all levels.
  • Opportunity to work in a small, fast-paced biotechnology company with a growing clinical pipeline.
  • Role combines strategic leadership with hands-on statistical expertise.

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