Senior RWE Analytics Engineer

Cytel

Des Moines (IA)

On-site

USD 120,000 - 150,000

Full time

14 days+
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Job summary

Cytel Inc. is seeking a senior epidemiology statistician to design and conduct real-world data analyses. You will collaborate with epidemiologists and statisticians to develop analytic plans, code data, and create datasets from large claims/EHR sources for observational studies.

You will apply regression, survival, and propensity methods, present findings to clients, and contribute to regulatory/safety documents and study reports. The role emphasizes cross-functional teamwork and timely delivery.

Qualifications

  • Master’s degree or PhD in related field (epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of RWE analytics experience in pharma, CRO, or academia.
  • Intermediate to expert SQL proficiency required; SAS or R proficiency required.
  • Deep expertise analyzing RWE data sources such as Optum Clinformatics, Truveta, UK Biobank; experience with clinical trial/registry data.

Responsibilities

  • Assist in development of study protocols and analysis plans using large RWD sources (claims and/or EHR).
  • Liaise with data vendors to obtain data extracts for research studies.
  • Create analytical databases to facilitate analyses; conduct analyses per study protocols.
  • Produce tables/figures for discussions with investigators/clients and study reports.
  • Present results internally and to clients; assist in study report preparation; potential supervisory duties.

Skills

SQL proficiency
SAS or R proficiency
RWE analytics
Project management
Communication
Stakeholder management

Education

Master’s or PhD in epidemiology/biostatistics/statistics/bioinformatics/economics

Tools

SQL
SAS
R
Relational databases

Job description

Cytel Inc. is seeking a senior epidemiology statistician to design and conduct real-world data analyses. You will collaborate with epidemiologists and statisticians to develop analytic plans, code data, and create datasets from large claims/EHR sources for observational studies.

You will apply regression, survival, and propensity methods, present findings to clients, and contribute to regulatory/safety documents and study reports. The role emphasizes cross-functional teamwork and timely delivery.

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