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6 часов назад

Senior Statistical Programmer (Biotechnology)

135 000 - 150 000$
Формат работы
remote (только USA)/onsite
Тип работы
fulltime
Грейд
senior
Английский
c1
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 (SAS/Clinical Trials): Leading the creation, validation, traceability, reproducibility, and maintenance of clinical trial analysis datasets and statistical outputs with an accent on regulatory submissions, CDISC standards, and programming quality. Focus on solving complex statistical programming tasks, developing reusable macros, standardizing data processes, and mentoring junior programmers.

Location: Onsite in Dunkirk, NY, or remote depending on the candidate’s geographic location. Regular schedule is Monday–Friday during standard business hours, with flexibility subject to manager approval.

Annual base pay: $135,000–$150,000 for the national market. Premium-market range: $144,000–$160,000 annually. The position is also eligible for a discretionary bonus and equity award.

Company

hirify.global is a publicly traded biotechnology company developing immunotherapies, cell therapies, cancer vaccines, and treatments for infectious diseases.

What you will do

  • Lead statistical programming activities for clinical trial analysis datasets and statistical outputs, including creation, validation, traceability, reproducibility, and maintenance.
  • Contribute to and review statistical analysis plans and analysis dataset specifications.
  • Prepare electronic submissions of clinical trial data for regulatory authorities.
  • Provide solutions for complex programming tasks and support resource planning across concurrent projects.
  • Lead or contribute to data standardization, including CRF and database design, edit checks, CDISC STDM/ADaM standards, and e-submissions.
  • Develop and validate global programming macros, improve processes, and mentor and train junior staff.

Requirements

  • Bachelor’s degree in Statistics, Biostatistics, Computer Science, Mathematics, or a related field with 7+ years of relevant experience, or a master’s degree with 5+ years of relevant experience.
  • 5+ years of statistical programming experience in the pharmaceutical industry is preferred.
  • Strong programming skills and high proficiency in SAS.
  • Experience as a lead statistical programmer on several concurrent projects.
  • Working knowledge of clinical research, Good Clinical Practices, regulatory requirements, and CDISC STDM/ADaM guidelines.
  • Excellent English verbal and written communication skills, along with strong organizational and interpersonal skills.

Culture & Benefits

  • Collaborative environment with opportunities to work across different company areas.
  • Professional development opportunities within a growing company.
  • Medical, dental, and vision plan options, health and financial wellness programs, and an employee assistance program.
  • Life, disability, flexible spending, 401(k) with company match, and 529 education savings benefits.
  • Paid time off, holidays, wellness resources, legal services, identity theft protection, pet insurance, and employee discounts.

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