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3 дня назад

Associate Statistical Programming Director

165 500 - 235 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
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
Associate Statistical Programming Director (SAS/R, Biotech): Leads statistical programming for clinical studies and projects, developing standardized datasets, analysis programs, macros, and regulatory submission components with an accent on CDISC standards, data quality, and CRO oversight. Focus on coordinating study programming, designing reusable statistical tools, and ensuring accurate, compliant outputs for pharmaceutical and biotech analyses.

Location: Alameda, California, United States; onsite office-based role

Salary: $165,500–$235,500 annually

Company

hirify.global operates in the pharmaceutical and biotechnology field, supporting clinical development and regulatory submissions through statistical programming.

What you will do

  • Lead statistical programming activities at the study and project level using SAS and R.
  • Maintain the macro library, develop global macros and standard programs, and create training and documentation materials.
  • Develop SDTM, ADaM, ODS, analysis datasets, listings, tabulations, graphical summaries, and statistical estimates.
  • Coordinate data transfers and required outputs with clinical data management and biostatistics teams.
  • Oversee CRO dataset development and perform programming quality control of tables, listings, figures, and analysis datasets.
  • Coordinate programming resources, support department infrastructure, troubleshoot issues, and help meet study timelines.

Requirements

  • BS/BA with at least 11 years of related experience, MS/MA with at least 9 years, PhD with at least 5 years, or an equivalent combination.
  • At least 8 years of pharmaceutical or biotechnology programming experience.
  • Demonstrated proficiency in R, SAS/Base, SAS/Stat, and SAS/Macros.
  • Extensive experience in the relevant profession and specialization, with the ability to resolve complex issues and lead work performed by others.
  • Strong analytical, written, verbal, and business communication skills.
  • Ability to work from the Alameda, California office.

Nice to have

  • UNIX, CDISC, and SAS graphics experience.
  • Experience with oncology clinical trials.
  • NDA submission experience.
  • Certification in the assigned area.

Culture & Benefits

  • Collaborative office environment with equipment including dual monitors and ergonomic chairs.
  • 401(k) plan with company contributions.
  • Medical, dental, vision, life, disability, and flexible spending account benefits.
  • Annual bonus eligibility and opportunities to purchase company stock and receive long-term incentives.
  • 15 accrued vacation days in the first year, 17 paid holidays, a company-wide winter shutdown, and up to 10 sick days annually.

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