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Sr. Manager, Biostatistician / Programmer (Clinical Trials)

Формат работы
hybrid
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
Sr. Manager, Biostatistician / Programmer (Clinical Trials): Developing and validating statistical programming deliverables for clinical trials, including Tables, Figures, Listings, analysis datasets, and exploratory analyses with an accent on clinical data standards, SAS programming, and scientific interpretation. Focus on interrogating trial data, supporting oncology and cell therapy programs, leveraging AI-assisted programming, and improving reproducibility across studies.

Location: Hybrid role based in Somerset, New Jersey, United States. Applicants must be authorized to work in the United States.

Company

hirify.global is a global biotechnology company developing cell therapies, including CAR-T, TCR-T, and natural killer cell-based treatments for serious diseases.

What you will do

  • Develop, validate, and maintain Tables, Figures, and Listings for clinical trials, interim analyses, and internal or external deliverables.
  • Perform hands-on statistical programming, data manipulation, exploratory analyses, and ad hoc analyses.
  • Interrogate clinical trial data to identify trends, anomalies, and insights for clinical decision-making.
  • Collaborate with Biostatistics, Clinical Development, Clinical Operations, Data Management, Translational Research, and Medical teams.
  • Contribute to analysis datasets, programming specifications, documentation, quality control, and regulatory-compliant deliverables.
  • Improve programming efficiency, standardization, and reproducibility across studies and programs.

Requirements

  • Master’s degree or PhD in Statistics, Biostatistics, Mathematics, Data Science, or a related quantitative discipline.
  • Hands-on experience developing TFLs and performing ad hoc and exploratory analyses for clinical trials.
  • Strong understanding of clinical trial design, clinical data structures, therapeutic context, and clinical endpoints.
  • Advanced proficiency in SAS and working knowledge of R for exploratory analyses and data visualization.
  • Strong experience with clinical data standards such as SDTM and ADaM.
  • US work authorization is required; employment eligibility will be verified through E-Verify.

Nice to have

  • Experience supporting oncology and/or cell therapy programs.
  • Experience with or strong willingness to use AI-assisted programming tools.

Culture & Benefits

  • Work in a fast-moving biotechnology environment with a high degree of autonomy.
  • Permanent full-time employees are eligible for hirify.global benefits.
  • Contractors are not eligible for benefits through hirify.global.

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