Senior RWE Programmer for Epidemiology Analytics

Cytel

Juneau (AK)

On-site

USD 120,000 - 180,000

Full time

9 days ago

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Job summary

Cytel Inc. is seeking a senior epidemiology statistician to advance real-world data analytics and support regulatory/submission activities.

You will collaborate with Epidemiology, Medical Affairs, and Safety teams to translate RWD into actionable study insights, develop analysis plans, and implement robust statistical methods. The ideal candidate holds a Master’s or PhD with 5+ years of RWE analytics experience in pharma/CRO/academic settings, strong SQL, SAS or R skills, and a track record of

Qualifications

  • Master’s degree in epidemiology, biostatistics, statistics, bioinformatics, economics or related field.
  • 5+ years of experience conducting Real-World Evidence analytics for pharma, CRO, or academic institutions.
  • Intermediate to expert SQL; SAS or R proficiency required.
  • Experience with RWE data sources such as Optum Clinformatics Datamart, Truveta, UK Biobank is preferred.

Responsibilities

  • Assist in development of study protocols and analysis plans leveraging large RWD sources (Claims and/or EHR).
  • Liaise with data vendors to obtain relevant data extracts for research studies consistent with study protocols.
  • Create analytical databases from data extracts to facilitate conduct of data analyses.
  • Conduct analyses consistent with methods set forth in study protocols and analysis plans.
  • Produce tables and figures for discussions with other investigators, clients, and for study reports.
  • Present results internally and to clients.
  • Assist in the preparation of study reports and other deliverables.
  • May have supervisory responsibilities in the future.

Skills

SQL
SAS
R
Data analysis
Project management
Communication

Education

Master's or PhD in a related field

Tools

Optum Clinformatics Datamart
Truveta
UK Biobank

Job description

Cytel Inc. is seeking a senior epidemiology statistician to advance real-world data analytics and support regulatory/submission activities.

You will collaborate with Epidemiology, Medical Affairs, and Safety teams to translate RWD into actionable study insights, develop analysis plans, and implement robust statistical methods. The ideal candidate holds a Master’s or PhD with 5+ years of RWE analytics experience in pharma/CRO/academic settings, strong SQL, SAS or R skills, and a track record of

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