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4 дня назад

Director, Biostatistics

Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
UK
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
Director, Biostatistics (clinical trials/statistical programming): Leading rigorous statistical design, analysis, interpretation, and regulatory submission support for global clinical development projects in inflammation and immunology with an accent on clinical trial methodology, cross-functional leadership, and reproducible statistical programming. Focus on designing statistical analysis plans, synthesizing results across studies, supporting regulatory deliverables, and applying innovative statistical methods.

Location: United Kingdom - Walton Oaks. Applicants must have authorization to live and work in the UK.

Company

hirify.global is a pharmaceutical company focused on developing medicines and digital solutions that improve patient health outcomes.

What you will do

  • Lead statistical planning and provide scientifically rigorous input into clinical study design, statistical analysis plans, and project development plans.
  • Oversee clinical trial conduct, data management, statistical analysis, interpretation of results, and study-level deliverables.
  • Prepare statistical analyses, data presentations, scientific reports, publications, regulatory submissions, and product defense materials.
  • Provide statistical leadership across clinical, regulatory, medical, data management, programming, and commercial functions.
  • Manage contract biostatisticians when required, including resource allocation, work scheduling, and project status monitoring.
  • Participate in research on innovative statistical methodologies and their applications to drug development.

Requirements

  • Master's degree in Statistics, Biostatistics, or a related field with extensive clinical trial experience, or a PhD with notable clinical trial experience.
  • Relevant clinical trial and business experience covering clinical, regulatory, and marketing operations.
  • Strong statistical skills, complex data analysis capability, and experience providing statistical leadership to cross-functional teams.
  • Proficiency in R, SAS, or Python and experience with a reproducible research tool such as R Markdown, Quarto, or Git/GitHub.
  • Strong verbal and written communication skills for collaboration with internal and external stakeholders.
  • Relevant authorization to live and work in the UK is required.

Nice to have

  • Experience influencing and collaborating with peers, developing and coaching others, and overseeing colleagues' work.

Culture & Benefits

  • Patient-centric culture guided by courage, joy, equity, and excellence.
  • Digital transformation initiatives using data, modelling, and automated solutions to accelerate drug discovery and development.
  • Flexible workplace culture supporting work-life harmony.
  • Commitment to diversity, inclusion, accessibility, and reasonable workplace adjustments.

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