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4 дня назад

Manager, Statistics (Clinical Trials)

Формат работы
onsite
Тип работы
fulltime
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
Manager, Statistics (Clinical Trials): Designing, analyzing, and interpreting clinical trials and observational studies for clinical development, regulatory submissions, HTA, and evidence generation with an accent on rigorous statistical methodology, real-world data, and compliance with regulatory requirements. Focus on delivering statistical analysis plans, study and submission outputs, cross-functional leadership, and communicating results to scientific, regulatory, and professional audiences.

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

Company

hirify.global develops medicines and applies data, modelling, and automated solutions to accelerate drug discovery and development and improve health outcomes.

What you will do

  • Design, analyze, and interpret clinical trials and observational studies in line with regulatory requirements, hirify.global standards, and statistical best practices.
  • Provide statistical expertise for clinical development, publications, presentations, evidence generation, regulatory submissions, and Health Technology Assessment submissions.
  • Develop statistical analysis plans, interpret results, and deliver clinical trial, exploratory, and meta-analysis reports and presentations.
  • Own study-, project-, and submission-level statistical deliverables, ensuring quality and timely delivery.
  • Provide statistical leadership and collaborate with clinical, regulatory, payer, programming, academic, and other cross-functional partners.
  • Contribute to statistical methodology research and strengthen the statistics community through collaboration, scholarship, presentations, and learning.

Requirements

  • Advanced degree in statistics, biostatistics, or a related field.
  • Relevant experience with clinical trials, real-world data, and business processes related to clinical, regulatory, and marketing operations.
  • Ability to provide statistical leadership to cross-functional teams at protocol and project level.
  • Strong statistical skills applied to clinical trials and/or observational studies.
  • Effective verbal and written communication skills.
  • Relevant authorisation to live and work in the UK.

Culture & Benefits

  • Patient-centric culture guided by courage, joy, equity, and excellence.
  • Flexible workplace culture supporting work-life harmony.
  • Commitment to diversity, inclusion, and reasonable adjustments for applicants with disabilities.
  • Full-time employment.

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