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7 дней назад

Senior Principal Scientist, Data Science RWE (Real-World Evidence)

137 000 - 235 750$
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
Senior Principal Scientist, Data Science RWE (Real-World Evidence): Leading real-world evidence projects and developing statistical and programming methods for external control arms, hybrid controls, comparative effectiveness analyses, and post-hoc clinical trial analyses with an accent on RWE study design, bias mitigation, and regulatory-grade evidence. Focus on building reusable tools, creating study protocols and statistical analysis plans, analyzing healthcare data sources, and mentoring data scientists.

Location: Hybrid role based in Titusville, New Jersey, United States of America. Additional posting locations include Cambridge, Massachusetts; Raritan, New Jersey; and Spring House, Pennsylvania.

Salary: $137,000–$235,750 per year, plus eligibility for incentive, retirement, and paid-leave programs.

Company

Johnson & Johnson MedTech and Innovative Medicine develop healthcare treatments, technologies, and solutions across the spectrum of patient care.

What you will do

  • Lead a portfolio of real-world evidence projects as a hands-on scientific and technical leader.
  • Develop best practices and maintain reusable tools that accelerate real-world data science delivery.
  • Design and execute end-to-end RWE studies, including research questions, feasibility, study design, analysis, programming, and interpretation.
  • Develop methods to mitigate observed and unobserved bias in external control arm, hybrid control, and comparative effectiveness studies.
  • Generate actionable insights from post-hoc RCT analyses, observational databases, and literature reviews for regulatory interactions.
  • Partner with therapeutic-area data scientists, mentor team members, and deliver protocols, statistical analysis plans, analysis-ready data, tables, and figures.

Requirements

  • Ph.D. in epidemiology or biostatistics.
  • Expert coding skills in R, Python, or SAS.
  • At least 5 years of relevant experience in biopharma, RWE consulting, or related healthcare industries.
  • Hands-on experience extracting, cleaning, and analyzing data, including methods for mitigating confounding and selection bias.
  • Expertise with multiple real-world data sources, including EHR, insurance claims, and registry data; familiarity with clinical trial data structures.
  • Excellent interpersonal, communication, presentation, and mentoring skills.

Nice to have

  • Familiarity with drug discovery and clinical development.
  • Subject matter knowledge in oncology, immunology, or neuroscience.
  • Experience producing regulatory-grade evidence and responding to agency reviews and comments.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo and equal opportunity principles.
  • Retirement pension and 401(k) savings plans.
  • Long-term incentive program eligibility.
  • Paid vacation, sick time, holidays, personal and family time, parental, bereavement, caregiver, volunteer, and military spouse leave.

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