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3 дня назад

Senior Statistical Programmer (SAS/R)

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

Текст:
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TL;DR
Senior Statistical Programmer (SAS/R): Leading statistical programming for clinical trials, including validated datasets, tables, figures, listings, and CDISC-compliant electronic submissions with an accent on SAS, R, clinical data standards, and cross-functional delivery. Focus on overseeing programming deliverables, supporting SDTM/ADaM specifications, managing vendors, and providing technical guidance to other programmers.

Location: United States; remote role

Company

hirify.global is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

  • Lead and support statistical programming activities for clinical trials.
  • Program and validate derived datasets, tables, figures, and listings using clinical trial data and external data sources.
  • Program and validate CDISC-compliant deliveries and support electronic submission documentation.
  • Contribute to CRF, Data Transfer Specification, Statistical Analysis Plan, SDTM, ADaM, and Define package development and review.
  • Oversee programming deliverables from CROs, internal contractors, and external vendors while ensuring timely, high-quality delivery.
  • Develop working instructions, guidelines, enhanced functions, macros, and utilities.

Requirements

  • Bachelor’s or master’s degree in Computer Science, Mathematics, Engineering, Medical, or a related discipline.
  • More than 5 years of statistical programming experience with a bachelor’s degree, or 3 years with a master’s degree, in the pharmaceutical industry.
  • Strong SAS and SAS Macro language skills, with working knowledge of SAS components.
  • Knowledge of R programming in clinical trials and familiarity with the drug development process.
  • Strong knowledge of industry standards and experience with data integrations such as ISS and ISE.
  • Strong oral and written communication skills, including the ability to explain analyses to less technical colleagues.

Culture & Benefits

  • Permanent position within an in-house team.
  • Projects supporting pharmaceutical, biotechnology, medical device, and consumer health clients.
  • Professional growth supported by continuous training and development.
  • One-team, quality-driven culture focused on diversity and inclusion.
  • Opportunity to contribute to the development and commercialization of innovative drugs and devices.

Hiring process

  • Submit a CV and receive an application acknowledgement.
  • Qualified candidates are invited to a phone interview as the first step.

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