> Markdown version of [/jobs/ext/3610059-senior-programmer-fsp-rwd-epi](https://www.wearedevelopers.com/jobs/ext/3610059-senior-programmer-fsp-rwd-epi). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Programmer FSP - RWD/EPI - **Company:** Cytel Inc. - **Location:** Waltham, MA, United States (Remote available) - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Bioinformatics, Computer Programming, Databases, Data Governance, Relational Databases, Generalized Linear Model, Regression Analysis, SAS (Software), SQL Databases - **Published:** October 7, 2026 - **Apply:** https://arc.dev/remote-jobs/j/redirect/pplejjqvls ## About the Role * 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. Experience analyzing clinical trial and/or registry data is required * 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 ## Description * Providing support to the Epidemiology team by preparing Real World data, advising on data analytic strategies, and supporting stakeholders in various epidemiology analytic activities * Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of statistical packages or platforms * Supporting statistical programming to generate innovative means of data standardization, visualization, and reporting of observational data * Supporting Medical Affairs (e.g. observational studies leveraging RWD); Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the development of regulatory/safety documents, and Clinical Development (e.g.; assessment of patient populations/ protocol feasibility) * The position will partner with Epidemiologists to manage relationships with internal and external stakeholders * Being able to prioritize and manage work across multiple projects and stakeholders * Providing strong communication to ensure successful and timely project delivery * Solving technical problems with experience and expertise Responsibilities Summary of Key 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