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Statistical Programmer (SAS)

46 000
Формат работы
remote (только Europe)/hybrid
Тип работы
fulltime
Грейд
senior/lead
Английский
c1
Страна
US/Europe/Italy
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
Statistical Programmer (SAS): Developing and validating SAS programs, clinical trial datasets, tables, listings, graphical outputs, and regulatory submission packages with an accent on CDISC standards, data integrity, and clinical and safety data systems. Focus on leading submission programming, building data-quality checks and reporting libraries, and overseeing complex programming activities performed by CROs.

Location: Europe (flexible) — remote or hybrid

Minimum salary: €46,000 annually for the Italy-based role; compensation in other countries follows the applicable local market and internal frameworks.

Company

Chiesi is an international research-focused biopharmaceutical group operating in more than 30 countries, with a focus on innovative medicines and rare diseases.

What you will do

  • Lead SAS programming activities for clinical, safety, and post-marketing data systems.
  • Develop, validate, and maintain SAS datasets, listings, tables, spreadsheets, graphical outputs, and reporting processes.
  • Prepare Case Report Tabulations, transport files, metadata, and other regulatory submission packages using CDISC standards.
  • Build standard SAS edit checks, data-quality processes, and libraries of reusable programming tools.
  • Contribute to Statistical Analysis Plans, mock-up table shells, TLFs, data warehouse activities, and SOP development.
  • Lead submission-related programming and oversee programming activities performed by CROs.

Requirements

  • Bachelor’s degree in Health Sciences, Statistics, Computer Science, or a related field; a Master’s degree is preferred.
  • More than 7 years of pharmaceutical or CRO experience.
  • Advanced SAS programming expertise and experience creating SAS reporting systems.
  • Solid understanding of data management, biostatistics, data integration, and data issue resolution.
  • In-depth knowledge of CDISC standards and regulatory requirements including GCP, GCDMP, and CFR 21.11.
  • Fluent English; strong organizational skills and the ability to manage multiple priorities independently and collaboratively.

Nice to have

  • SAS certification and/or A. Stat or P. Stat accreditation.
  • Master’s degree in a related field.

Culture & Benefits

  • Work in a sustainability-focused Benefit Corporation and certified B Corp.
  • Annual performance-based bonus scheme.
  • Pension, private medical insurance, wellbeing programme, and flexible benefits programme.
  • Flexible working arrangements, remote work options, tax assistance, and relocation support.
  • Access to training, development resources, healthcare programmes, and work-life balance initiatives.

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