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2 дня назад

Principal Biostatistician (Oncology)

227 500 - 284 400$
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
Principal Biostatistician (Oncology) (Clinical Trials/Oncology): Leading the design, analysis, and reporting of practice-changing oncology randomized clinical trials for molecular diagnostic tests with an accent on adaptive designs, biomarker-informed methodology, and advanced survival analysis. Focus on designing complex studies, evaluating endpoints and competing risks, developing statistical analysis plans, and mentoring biostatisticians.

Location: San Carlos, California, United States

Salary: $227,500–$284,400 USD annually, plus performance bonus and equity awards

Company

hirify.global develops molecular diagnostic and cell-free DNA testing products for oncology, women’s health, and organ health.

What you will do

  • Lead statistical design, analytical planning, and reporting for oncology clinical utility studies and randomized clinical trials.
  • Develop efficient study designs tailored to complex oncology use cases, including adaptive and biomarker-informed approaches.
  • Serve as study statistician for sponsored studies and provide statistical consulting for external collaborations.
  • Partner with clinical, medical, and translational scientists to plan and execute studies and address analytical risks.
  • Author and review statistical analysis plans, tables, listings, figures, clinical study reports, and publications.
  • Apply innovative statistical methods, improve analytical processes, and mentor early-career statisticians.

Requirements

  • Advanced degree in Biostatistics, Statistics, or a related quantitative field; Ph.D. preferred.
  • 15+ years of experience in clinical trial biostatistics.
  • Expertise in time-to-event analysis, censoring, competing risks, and advanced survival modeling in oncology.
  • Experience with adaptive and biomarker-informed study designs, power calculations, sample size determination, and endpoint evaluation.
  • Working knowledge of ICH and GCP guidelines and CDISC standards, including SDTM and ADaM.
  • Proficiency in R and the ability to communicate complex statistical concepts to technical and non-technical audiences.

Nice to have

  • Working knowledge of NGS-based diagnostics and ctDNA/MRD.
  • Experience with non-inferiority studies.

Culture & Benefits

  • Comprehensive medical, dental, vision, life, and disability benefits.
  • 401(k) with company match.
  • Annual performance incentive bonus and long-term equity awards.
  • Paid time off, company holidays, pregnancy and baby bonding leave, commuter benefits, and wellness programs.
  • Employees and immediate family members receive free testing and fertility care benefits.

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