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5 дней назад

Senior Data Scientist I (RWE)

120 000 - 170 000$
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

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TL;DR
Senior Data Scientist I (RWE) (Real-World Evidence and Oncology): Leading observational studies and RWE analyses for pharmaceutical partners using complex clinical, molecular, claims, EHR, and registry data with an accent on survival analysis, causal inference, and oncology study design. Focus on deriving real-world endpoints, building reusable analytical standards, and applying LLMs and agentic workflows to accelerate scientific analysis and documentation.

Location: Boston, United States

Salary: $120,000–$170,000 annually for the listed California range; $130,000–$180,000 for NYC/SF. Compensation may vary by location, qualifications, and experience.

Company

hirify.global develops an AI-enabled real-world evidence platform connecting clinical and molecular data to support precision medicine and healthcare decision-making.

What you will do

  • Lead the design and delivery of real-world evidence analyses for pharmaceutical clients.
  • Translate drug development questions into research plans for trial design and outcomes research.
  • Derive complex real-world endpoints from clinical and molecular datasets using extensive coding.
  • Develop methodological standards, reusable code, and internal analytical packages.
  • Apply LLMs, agentic workflows, and other AI tools to accelerate coding, review, documentation, and insight generation.
  • Interpret and communicate analytical results, limitations, and study implications to technical and non-technical stakeholders.

Requirements

  • Education in epidemiology, biostatistics, data science, public health, or a related field: PhD with 2+ years of additional experience, or master's degree with 4+ years of additional experience.
  • Expertise with observational real-world healthcare data and time-to-event methodologies, including survival analysis.
  • Proficiency in R and SQL, statistical tools and packages, machine learning, and LLM-based coding assistants or agentic frameworks.
  • Experience with software engineering practices, version control, modular code, documentation, and code review.
  • Client-facing communication experience, strong presentation skills, and the ability to work with multidisciplinary scientific teams.

Nice to have

  • Pharmaceutical, drug development, or Phase II–III clinical trial design experience.
  • Experience analyzing claims, EHR, registry, biomarker, genomic, or other high-dimensional molecular data.
  • Experience building or configuring LLM-based tools and agentic workflows for scientific discovery.
  • Knowledge of oncology guidelines such as NCCN.
  • Experience with AWS, BigQuery, or Google Cloud Platform.

Culture & Benefits

  • Collaboration with product, oncology, clinical abstraction, and real-world data science teams.
  • Opportunity to contribute to data quality, product development, and analytical best practices.
  • Benefits may include incentive compensation, restricted stock units, medical coverage, and other benefits depending on the position.
  • Equal opportunity employment with consideration under applicable fair-chance employment laws.

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