Назад
Company hidden
10 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
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Senior Director, Biostatistics (Biotechnology): Leading statistical strategy and execution across preclinical and clinical development programs with an accent on complex study design, data analysis, regulatory submissions, and biometrics oversight. Focus on applying advanced statistical methods, managing CROs and cross-functional teams, and solving data, resourcing, and compliance challenges across a clinical-stage therapeutic pipeline.

Location: South San Francisco, United States; on-site at least three days per week

Salary: $250,000–$300,000 per year

Company

Clinical-stage biotechnology company developing therapies for genetically validated cardioendocrine diseases, including severe hypertriglyceridemia and acromegaly.

What you will do

  • Lead statistical planning, analysis, and interpretation across preclinical and clinical development programs.
  • Represent biostatistics on clinical study teams and develop strategic statistical approaches aligned with regulatory and industry standards.
  • Define and oversee best practices for scientific and clinical data handling, analysis, and interpretation.
  • Oversee CROs, biometrics vendors, consultants, statisticians, programmers, and data managers.
  • Support global regulatory strategy, submissions, scientific publications, and regulatory interactions.
  • Assess biometrics risks, resourcing, infrastructure, and execution, providing updates to cross-functional and leadership teams.

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.
  • Experience leading teams and vendors across statistics, programming, and data management.
  • In-depth knowledge of all phases of global drug development and regulatory submission processes.
  • Ability to work cross-functionally, manage projects under pressure, and communicate effectively with diverse stakeholders.
  • 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.
  • Experience supporting scientific publications and communications strategies.

Culture & Benefits

  • Collaborative, hands-on environment with direct contribution expected at every level.
  • Opportunity to work with a dynamic team advancing a clinical-stage therapeutic pipeline.
  • Role combines strategic leadership with hands-on statistical expertise.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →