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5 дней назад

Principal Statistical Programmer (SAS)

149 200 - 223 800$
Формат работы
remote (только USA)/hybrid/onsite
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
Principal Statistical Programmer (SAS): Leading statistical programming for clinical development and regulatory submissions with an accent on advanced SAS, clinical trial reporting, CDISC standards, and eCTD deliverables. Focus on solving complex clinical trial reporting problems, quality-controlling statistical programming outputs, and coordinating cross-functional submission activities under FDA, ICH, and GCP requirements.

Location: Boston, MA, United States. The role is remote-eligible, with remote, hybrid, or on-site work arrangements available under the company flex program.

Salary: $149,200–$223,800 annually, plus eligibility for an annual bonus and equity awards.

Company

Vertex is a global biotechnology company focused on scientific innovation.

What you will do

  • Lead statistical programming activities for clinical sub-teams and delegate work while tracking progress.
  • Develop and use advanced SAS programs, including SAS Macro, BASE SAS, SAS/STAT, and SAS/GRAPH.
  • Perform quality control of SAS code and outputs produced by other Statistical Programmers.
  • Solve complex clinical trial reporting problems and support accurate, timely study execution.
  • Create analyses, files, and documentation for electronic submissions in eCTD format, including ISS and ISE.
  • Coordinate with Statistical Programming, Biostatistics, Data Management, and other submission-related functions on reporting, process improvement, and technology initiatives.

Requirements

  • Bachelor’s degree in a scientific discipline.
  • Typically 8+ years of experience with a bachelor’s degree, or 5+ years with an M.S. or higher, in biotechnology, pharmaceuticals, or a clinical research organization.
  • Strong proficiency in SAS programming, procedures, and functions used in clinical trial reporting.
  • Intermediate knowledge of CDISC standards and clinical trials.
  • Experience with regulatory submissions and FDA/ICH/GCP compliance.
  • Effective written and verbal communication skills for explaining complex information.

Culture & Benefits

  • Choice of remote, hybrid, or on-site work under the Flex @ Vertex program.
  • Medical, dental, and vision benefits.
  • Generous paid time off, including week-long summer and winter company shutdowns.
  • Educational assistance programs, including student loan repayment.
  • Commuting subsidy, matching charitable donations, and 401(k).

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