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10 дней назад

Senior Statistical Programmer (SAS)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Kenya
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): Designing and delivering submission-ready ADaM datasets, tables, figures, listings, and clinical data packages with an accent on SAS programming, R programming, CDISC standards, and regulatory submission readiness. Focus on leading pooled and exploratory analyses, developing complex SAS programs, and building global tools for clinical statistical programming.

Location: Nairobi, Kenya

Company

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

What you will do

  • Design and deliver submission-ready ADaM datasets, tables, figures, listings, and analysis submission packages.
  • Develop and quality-control SAS programs for accessing, transforming, analyzing, and reporting clinical trial data.
  • Lead pooled and exploratory analyses across multiple clinical studies in collaboration with statisticians and clinical programming teams.
  • Oversee the development of ISS and ISE datasets and related outputs.
  • Develop global programming tools that improve the efficiency and capacity of the Statistical Programming group.
  • Support regulatory responses, integrated safety and efficacy summaries, publications, presentations, and clinical trial planning.

Requirements

  • BSc in Computer Science, Mathematics, Statistics, or a related field, with relevant experience.
  • At least 5 years of clinical or statistical programming experience in a CRO or pharmaceutical environment.
  • Extensive experience with SAS, including SAS Macro development and use.
  • Hands-on experience with R programming is mandatory.
  • Advanced knowledge of CDISC standards, including CDASH, SDTM, and ADaM.
  • Experience leading pooled and exploratory analyses, submission activities, and cross-functional international clinical trial teams.

Culture & Benefits

  • Work with cross-functional, multicultural, and international clinical trial teams.
  • Operate in a role focused on high-quality, submission-ready clinical data deliverables.
  • Manage personal timelines while working independently and collaboratively.

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