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13 дней назад

Senior Statistical Programmer/Analyst Consultant (Oncology)

Формат работы
remote (только USA)
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
Senior Statistical Programmer/Analyst Consultant (Oncology) (SAS/CDISC): Leading statistical programming for oncology clinical studies from study start-up through database lock, analysis, and reporting with an accent on SAS programming, CDISC-compliant SDTM and ADaM datasets, and clinical trial reporting. Focus on developing and validating TLFs, supporting regulatory submissions, independently managing programming deliverables, and mentoring junior programmers.

Location: Remote in the United States

Company

hirify.global is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

  • Lead statistical programming activities for oncology clinical studies from study start-up through database lock, analysis, and reporting.
  • Develop, review, and maintain SAS programs for SDTM, ADaM, tables, listings, and figures.
  • Lead interim and final efficacy and safety analyses and support regulatory submissions.
  • Develop and review programming specifications in alignment with protocols, statistical analysis plans, and study methodology.
  • Generate and validate clinical trial outputs, datasets, and clinical study report deliverables.
  • Coordinate study-level programming activities, communicate risks and timelines, and mentor statistical programmers.

Requirements

  • Must be based in the United States; remote work is available within the US.
  • Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.
  • Significant experience in oncology clinical trials and strong experience in clinical trial statistical programming.
  • Strong proficiency in SAS, including Base SAS and procedures used for clinical trial reporting.
  • Strong knowledge of CDISC standards, particularly SDTM and ADaM, with experience developing and validating TLFs.
  • Experience with complex clinical trial data, regulatory submissions, independent programming delivery, and cross-functional collaboration.

Nice to have

  • Basic or working knowledge of R programming.
  • Experience in a CRO, pharmaceutical, or biotechnology environment.

Culture & Benefits

  • Work directly with a single sponsor while receiving the support and career opportunities of a global CRO.
  • Professional development supported through continuous training and mentorship.
  • Client-facing work with an emphasis on independent ownership and high-trust collaboration.
  • Inclusive workplace with a focus on diversity and equal opportunity.

Hiring process

  • Submit a CV and receive an application acknowledgement.
  • Qualified candidates are invited to a phone interview as the first step.

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