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9 дней назад

Principal Statistical Programmer, R Programming

98 200 - 273 200$
Формат работы
onsite
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

Текст:
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TL;DR
Principal Statistical Programmer, R Programming (Clinical Trials/R): Developing and validating R packages, R-Shiny applications, and submission-ready statistical outputs for clinical trial analysis with an accent on CDISC data structures, ADaM, TLFs, and data visualization. Focus on leading R implementation, building complex clinical data applications, and ensuring safety and efficacy outputs are accurate and submission-ready.

Location: Durham, North Carolina, United States of America

Salary: $98,200–$273,200 annual base pay

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Develop, update, and validate R packages for clinical trial analysis, including SDTM, ADaM, tables, figures, listings, submission packages, and data review.
  • Build complex R-Shiny applications, dashboards, and animations for clinical questions, Health Authority requirements, and decision-making.
  • Generate submission-ready statistical outputs using R Markdown and similar tools.
  • Lead R implementation and train other statistical programming team members.
  • Write and review application specifications and documentation while collaborating with clinical, statistical, and data management stakeholders.
  • Create and validate safety and efficacy outputs and global tools that improve the efficiency and capacity of statistical programming.

Requirements

  • Strong experience in R programming and package or application development for clinical trial data.
  • Strong programming skills in R, R Shiny, and R Markdown, including applying R and R Shiny to clinical trial analysis and reporting.
  • Strong data visualization and data wrangling skills, with proficiency in R packages for data exploration and visualization.
  • Knowledge of statistical methodology and clinical trial analysis.
  • Advanced knowledge of CDISC data structures and experience creating or validating ADaM and TLF outputs aligned with protocols, SAPs, aCRFs, and study documentation.
  • Experience with clinical trial and drug development studies is desirable.

Culture & Benefits

  • Full-time employment with base pay dependent on qualifications, location, and schedule.
  • Potential incentive plans, bonuses, and other compensation may be available.
  • Health and welfare benefits may be provided.
  • Equal opportunity employment and a commitment to integrity in the hiring process.

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