Note: The job is a remote job and is open to candidates in USA. Cytel is seeking a Senior Statistical Programmer to support epidemiology and real-world evidence analytics. The role involves preparing and analyzing real-world data, developing analytical databases, producing study outputs, supporting regulatory and safety deliverables, and collaborating with epidemiologists, clients, data vendors, and other stakeholders.
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
- Master's degree or PhD in related field (epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution
- Intermediate to expert level proficiency in SQL is a must
- In addition, SAS or R proficiency is required
- Deep expertise analyzing RWE data sources such as Optum (Clinformatics Datamart® and Market Clarity), Truveta and UK Biobank
- Familiarity with relational databases and proficient understanding of claims and ancillary file layouts
- Experience with applied statistics including regression analysis (OLS, longitudinal, logistic, Cox, GLM/GEE), survival analyses (Kaplan-Meier, cumulative incidence, accelerated failure time models), and propensity weighting
- Excellent project management skills; can prioritize multiple tasks and goals to ensure timely completion
- Confident and competent when interacting with internal and external stakeholders
- Strong written/verbal communication skills
- Highly effective at summarizing and presenting key considerations and evidence
- Experience analyzing clinical trial and/or registry data is desirable
Benefits
- Remote work arrangement
- Full-time employment
Company Overview
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