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5 дней назад

Data Scientist II (AI)

100 000 - 140 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Data Scientist II (AI): Leading real-world evidence studies for pharmaceutical partners using complex clinical and molecular data, with an accent on observational study design, survival analysis, oncology research, and AI-assisted analytical workflows. Focus on deriving real-world endpoints, applying causal and statistical methods, building reusable analytical code, and communicating findings to technical and non-technical stakeholders.

Location: Boston, United States

Salary: $100,000–$140,000 for CHI; $110,000–$150,000 for NYC/SF. Compensation may vary by location, qualifications, and experience.

Company

hirify.global develops a proprietary real-world evidence platform connecting clinical, molecular, and other healthcare data to support precision medicine and clinical decision-making.

What you will do

  • Partner with pharmaceutical collaborators to execute real-world evidence research plans for trial design and outcomes research.
  • Lead the derivation of complex real-world endpoints from clinical and molecular data.
  • Apply observational study methods, including causal inference and survival analysis, to real-world healthcare data.
  • Use LLMs, agentic workflows, and AI tools to accelerate coding, documentation, code review, and insight generation.
  • Interpret analytical results, assess study limitations, and communicate findings through reports, deliverables, manuscripts, and conference materials.
  • Collaborate with product, oncology, clinical abstraction, and real-world data science teams to improve data quality and analytical practices.

Requirements

  • PhD in epidemiology, biostatistics, data science, public health, or a related field; or a master’s degree with 2+ years of additional work experience.
  • Experience analyzing observational real-world healthcare data and executing real-world data studies.
  • Proficiency with R, SQL, statistical tools, and time-to-event methodologies such as survival analysis.
  • Experience applying machine learning, LLM-based coding assistants, and agentic frameworks to data analysis, code review, or scientific documentation.
  • Knowledge of software engineering practices, including version control, modular code, and documentation.
  • Strong client communication, presentation, project management, and cross-functional collaboration skills.

Nice to have

  • Pharmaceutical, drug development, or Phase II–III clinical trial design experience.
  • Experience with claims, EHR, registry, biomarker, molecular, or genomics data.
  • Knowledge of oncology guidelines such as NCCN and ongoing clinical trials.
  • Experience configuring or adapting LLMs for scientific work.
  • Experience with AWS, BigQuery, or Google Cloud Platform.

Culture & Benefits

  • Full-time employment with benefits that may include incentive compensation, restricted stock units, medical coverage, and other benefits.
  • Work with multidisciplinary scientists on complex healthcare and precision medicine problems.
  • Equal opportunity employment with consideration for qualified applicants with arrest or conviction records in accordance with applicable law.

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