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18 часов назад

Study Design Statistician (Medical Statistics)

Формат работы
remote (только USA)
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

Study Design Statistician (Medical Statistics): Leading the full life-cycle of clinical trial design and statistical services using KerusCloud with an accent on simulation, protocol preparation, and statistical analysis plans. Focus on designing complex trials, applying Bayesian approaches, and providing high-level statistical consultancy to pharmaceutical and biotech clients.

Location: Remote (USA)

Company

hirify.global is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with scientific approaches to complex trial data.

What you will do

  • Lead the full life-cycle of KerusCloud support and statistical services, from design to delivery.
  • Assist customers with study design, focusing on simulation to ensure alignment with study objectives.
  • Prepare study protocols and develop Statistical Analysis Plans (SAP) and Statistical Analysis Reports (SAR).
  • Summarize, analyze, and visualize study data using various statistical methods.
  • Provide statistical consultancy to sponsors across the full span of clinical development.
  • Collaborate with Product Development and Marketing to define KerusCloud features and conduct client demonstrations.

Requirements

  • Bachelor's degree in mathematics, statistics, physics, or pharmacology (Masters or PhD preferred).
  • 5-7 years of experience in the application of medical statistics within pharma, CRO, or academic settings.
  • Proficiency in SAS and/or R statistical software packages.
  • Must be based in the USA (implied by company location in Canton, MI).
  • Experience delivering customer projects to high quality standards.

Nice to have

  • Experience in study design, protocol writing, and report writing.
  • Experience with modelling and simulation techniques for complex study designs.
  • Knowledge of Bayesian approaches to the design and analysis of clinical data.
  • Experience with early-phase drug development processes and adaptive study designs.

Culture & Benefits

  • Work for a Great Place to Work certified organization known for exceptional culture.
  • Collaborative and inclusive work environment with an industry-leading employee retention rate.
  • Opportunity to work with state-of-the-art, proprietary cloud-based trial simulation software (KerusCloud).
  • Supportive and innovative team environment focused on shaping the future of clinical research.

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