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10 часов назад

Senior Manager, Biostatistics (Oncology)

170 000 - 204 750$
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 Manager, Biostatistics (Oncology) (Clinical Trials/Bayesian Statistics): Designing, analyzing, and interpreting clinical trials and experimental studies for biotechnology drug development with an accent on oncology endpoints, adaptive trial designs, and regulatory reporting. Focus on developing statistical analysis plans, performing advanced analyses in R, and mentoring biostatisticians and statistical programmers.

Location: Jersey City, New Jersey, United States

Salary: $170,000–$204,750 per year, plus bonus and equity compensation

Company

hirify.global Therapeutics is a biopharmaceutical company developing novel treatments using technologies that combine chemistry, engineering, computation, and biology.

What you will do

  • Collaborate with interdisciplinary teams to design clinical trials, experiments, and studies using appropriate statistical methodologies.
  • Lead statistical analysis plans covering endpoints, sample size determination, randomization strategies, and analytical methods.
  • Perform advanced analyses on complex datasets, interpret results, and draw actionable conclusions.
  • Provide statistical expertise for regulatory submissions and prepare relevant documentation.
  • Guide and mentor biostatisticians and statistical programmers.
  • Drive the implementation and use of advanced statistical tools and software.

Requirements

  • PhD or equivalent in statistics, biostatistics, or a related discipline with at least 3 years of clinical research and drug development experience, or a Master's degree with at least 7 years of relevant experience.
  • Deep hands-on proficiency in R and the Posit/RStudio ecosystem, including R Markdown, Shiny, and tidyverse.
  • Substantial oncology trial experience, including RECIST, dose-escalation or dose-optimization designs such as BOIN, and biomarker-driven subgroup analysis.
  • Ability to independently manage the full analysis lifecycle from raw data and exploratory analysis through final tables, listings, and figures.
  • Strong knowledge of ICH, FDA, and other regulatory guidelines, with experience authoring statistical analysis plans.
  • Experience with Bayesian statistics, adaptive trial designs, clinical publications or conference presentations, and leading or mentoring teams.

Culture & Benefits

  • Bonus and equity compensation in addition to base salary.
  • 401(k) plan with company matching.
  • Medical, dental, and vision insurance with substantial premium coverage.
  • Mental health and wellness benefits, enhanced parental leave, and generous paid time off.
  • Weeklong summer and winter holiday shutdowns.
  • Daily subsidized lunch when working on-site.

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