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14 дней назад

Senior Statistical Programmer Analyst - T (SAS)

65 - 115$
Формат работы
remote (только USA)
Тип работы
project
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 Analyst - T (SAS): Preparing clinical trial datasets, statistical analysis programs, and regulatory submissions with an accent on SAS programming, CDISC standards, and clinical data quality. Focus on developing analysis datasets, managing clinical data warehouses, building SAS macro libraries, and mentoring statistical programmers.

Location: Remote US home office; approximately 10% travel to conferences and hirify.global-affiliated facilities.

Salary: $65.00–$115.00 per hour.

Company

hirify.global is a global healthcare company that designs, develops, manufactures, and markets innovative medical devices and therapies.

What you will do

  • Develop SAS algorithms and programs for clinical datasets, listings, summary tables, graphs, and regulatory submissions.
  • Write specifications for analysis datasets based on statistical analysis plans.
  • Import, export, clean, transform, and analyze clinical trial data.
  • Manage clinical study data libraries and data warehouse metadata.
  • Collaborate with statisticians, programmers, data managers, regulatory affairs, quality assurance, and external clinical system vendors.
  • Mentor less experienced statistical programmers and act as a subject matter expert on CDISC and statistical programming practices.

Requirements

  • Bachelor’s degree in Statistics, Computer Science, or a related field, with 5+ years of statistical programming experience and 3+ years in clinical statistical programming within the medical device, biotechnology, pharmaceutical, or CRO industry.
  • Familiarity with Base SAS, SAS/GRAPH, SAS/ODS, and SAS/STAT.
  • Expertise in SAS data import, manipulation, analysis, export, graphics, SQL, and macro programming.
  • Knowledge of clinical data standards including CDASH, SDTM, ADaM, SHARE, BRIDG, ODM, Define, and controlled terminology.
  • Knowledge of clinical data management systems such as Oracle InForm and/or RAVE, international regulations, and clinical data requirements for regulatory submissions.
  • Strong communication skills, accuracy, attention to detail, multitasking ability, and proficiency with Microsoft Office tools.

Nice to have

  • SAS Base or Advanced Programmer certification.
  • Experience with metadata repositories and regulatory submissions.

Culture & Benefits

  • Collaborative environment with continuous learning and performance recognition.
  • Medical, dental, vision, life, AD&D, and short- and long-term disability insurance for eligible employees.
  • 401(k) with employer match, paid parental leave, paid holidays, accrued vacation, and paid sick time.
  • Work involves extended computer use in a general office environment and approximately 10% travel.

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