Senior RWD Epidemiology Programmer

Cytel; Topeka (KS); Vor Ort; USD 120.000 - 170.000; Vollzeit

Zusammenfassung

Cytel Inc. is seeking an experienced epidemiology/RWE analyst to prepare Real World data, advise on analytic strategies, and support stakeholders across regulatory and research activities.

You will program and conduct statistical analyses, develop data standards, create visualizations and reporting for observational data, and collaborate with Medical Affairs and safety teams to support regulatory documents and clinical development plans.

Qualifikationen

• Master’s degree or PhD in epidemiology, biostatistics, statistics, bioinformatics or economics with 5+ years of RWE analytics experience
• Proficiency in SQL; SAS or R required
• Deep expertise analyzing RWE data sources such as Optum Clinformatics Datamart, Truveta and UK Biobank
• Familiarity with relational databases and claims data layouts
• Experience with applied statistics including regression, survival analysis, and propensity weighting
• Excellent project management and stakeholder communication skills

Aufgaben

• 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
• Create analytical databases from data extracts to support analyses
• Conduct analyses per study protocols and analysis plans
• Produce tables/figures for discussions with investigators and clients
• Present results internally and to clients
• Assist in preparing study reports and deliverables
• May assume supervisory responsibilities in the future

Kenntnisse

SQL

SAS

R

Statistical analysis

Project management

Ausbildung

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

Tools

Optum Clinformatics Datamart

Truveta

UK Biobank

Jobbeschreibung

Cytel Inc. is seeking an experienced epidemiology/RWE analyst to prepare Real World data, advise on analytic strategies, and support stakeholders across regulatory and research activities.

You will program and conduct statistical analyses, develop data standards, create visualizations and reporting for observational data, and collaborate with Medical Affairs and safety teams to support regulatory documents and clinical development plans.