9 дней назад
Principal Statistical Programmer, R Programming
98 200 - 273 200$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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