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6 дней назад

Senior Statistical Programmer Analyst (SAS/R)

80 - 95CAD
Формат работы
remote (только Canada)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Canada
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 (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, and pharmaceutical industry standards. Focus on overseeing programming deliverables, designing SDTM/ADaM specifications, managing vendor contributions, and supporting high-quality data integrations and regulatory submissions.

Location: Mississauga, Ontario, Canada; remote work indicated.

Salary: $80–$95 CAD base salary range.

Company

hirify.global is a global full-service contract research organization supporting 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 from internal and external sources.
  • Program and validate CDISC-compliant deliveries and supporting documentation for electronic submissions.
  • Contribute to CRF, data transfer specification, statistical analysis plan, SDTM, ADaM, and Define package design and review.
  • Oversee CRO programming deliverables and help manage internal contractors and external vendors.
  • Develop working instructions, guidelines, macros, enhanced functions, and utilities.

Requirements

  • More than 5 years of statistical programming experience with a bachelor’s degree, or 3 years with a master’s degree, in a relevant discipline.
  • Strong SAS, SAS Macro language, and R programming skills applied to clinical trials.
  • Knowledge of pharmaceutical industry standards, the drug development process, and CDISC-related deliverables.
  • Experience leading statistical programming activities and providing technical guidance to other programmers.
  • Ability to work on ISS and ISE data integrations.
  • Strong oral and written communication skills, including the ability to explain analyses to less technical colleagues.

Culture & Benefits

  • Permanent role within an in-house team.
  • Projects span pharmaceutical, biotechnology, medical device, and consumer health clients.
  • Quality-driven one-team culture with a focus on professional growth.
  • Inclusive, barrier-free recruitment and selection process with accommodations available upon request.

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