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2 дня назад

Junior Statistician (Clinical Research)

Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
junior
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
Junior Statistician (Clinical Research): Supporting the design, analysis, and reporting of clinical trial data with an accent on statistical analysis plans, tables, listings, figures, and data quality checks. Focus on performing supervised statistical analyses, reviewing clinical data, contributing to study reports, and collaborating with statisticians, programmers, and cross-functional teams.

Location: United States; remote role. Visa sponsorship is not available.

Company

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

What you will do

  • Support senior statisticians in the design and analysis of clinical studies.
  • Assist with statistical analysis plans, table/listing/figure specifications, and related documentation.
  • Perform basic statistical analyses under guidance and review clinical trial data for discrepancies.
  • Prepare and review statistical tables, listings, figures, study reports, and clinical study reports.
  • Support statistical programming activities and collaborate with programmers, data managers, and other cross-functional teams.
  • Maintain study documentation and communicate progress, issues, and timelines in project meetings.

Requirements

  • Master’s degree in Statistics, Biostatistics, Mathematics, or a related quantitative discipline preferred; a bachelor’s degree with relevant experience may be considered.
  • 0–2 years of experience in statistics, biostatistics, or clinical research.
  • Basic understanding of statistical concepts and methodologies.
  • Analytical, problem-solving, organizational, communication, and teamwork skills.
  • Familiarity with clinical trial processes and pharmaceutical or biotechnology research.
  • Exposure to SAS, R, or Python is advantageous.

Nice to have

  • Exposure to clinical trial data and CDISC standards, including SDTM and ADaM.
  • Basic knowledge of clinical study design and statistical methods.
  • Experience with statistical programming or clinical data.

Culture & Benefits

  • Opportunity to work on global clinical research projects.
  • Exposure to experienced statisticians and cross-functional teams.
  • Professional development and career growth opportunities.
  • Collaborative and learning-oriented work environment with continuous training.

Hiring process

  • Application acknowledgement is sent after CV submission.
  • Qualified candidates are invited to a phone interview as the first step.

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