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5 дней назад

Senior Scientist, Biostatistics (AI)

109 000 - 174 800$
Формат работы
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
Senior Scientist, Biostatistics (AI) (Biostatistics/Clinical Development): Designing and executing statistical studies, experiments, and clinical trial analyses for pharmaceutical research and development with an accent on advanced statistical methods, reproducible R-based modeling, and regulatory-compliant evidence generation. Focus on optimizing study designs, performing simulations and sample size calculations, solving complex statistical and regulatory problems, and communicating findings across interdisciplinary drug development teams.

Location: Onsite at an office in Spring House, Pennsylvania; Titusville or Raritan, New Jersey; San Diego, California; or Cambridge, Massachusetts. No remote option.

Salary: $109,000–$174,800 annually, plus eligibility for an annual performance bonus.

Company

Johnson & Johnson MedTech and Innovative Medicine develop healthcare solutions, medicines, and medical technologies aimed at preventing and treating complex diseases.

What you will do

  • Design and execute statistical studies, experiments, and clinical trial analyses across Clinical Development, Medical Affairs, Discovery, and Manufacturing Sciences.
  • Apply statistical methodology, simulations, sample size calculations, and innovative data-adaptive approaches to optimize study and trial designs.
  • Use R as the primary programming language for modeling, visualization, data wrangling, document authoring, and evaluation, with SAS and other computational tools.
  • Interpret, report, and communicate data evidence for research, development, marketed products, publications, and regulatory submissions.
  • Represent Statistics & Decision Sciences in cross-functional teams and collaborate with quantitative scientists, clinical pharmacology experts, CROs, consultants, and regulatory stakeholders.
  • Manage projects end to end, support troubleshooting and health authority requests, contribute to process improvements, and supervise contractors, interns, or co-ops as needed.

Requirements

  • Ph.D. in Statistics or a related field with relevant experience, or a Master’s degree in Statistics or a related field with commensurate experience.
  • Proficiency in SAS and R programming, with experience using other relevant computational tools such as Python.
  • Experience applying statistical methods to studies, experiments, trials, or pharmaceutical research and development.
  • Strong written, verbal, interpersonal, and interdisciplinary communication skills in English.
  • Ability to produce accurate, reproducible analyses and statistical reports while managing multiple projects independently.
  • Ability to work onsite at one of the listed U.S. office locations; travel of less than 10% is anticipated.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo and commitment to diversity and dignity.
  • Medical, dental, vision, life insurance, disability, business accident, and group legal insurance programs may be available.
  • Eligibility for pension and 401(k) savings plans may be available.
  • Vacation, sick time, holiday pay, and work, personal, and family time benefits are provided according to applicable plans.
  • Opportunities to publish research, present at professional forums, participate in professional organizations, and develop statistical and computational expertise.

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