[Remote] Statistical Analytical Programmer

Note: The job is a remote job and is open to candidates in USA. Slipstream Life Sciences is focused on providing managed IT solutions for emerging pharma and biotech organizations. The Statistical Analytical Programmer will play a crucial role in transforming complex EMR-focused real-world data into analysis-ready datasets and high-quality study outputs, collaborating with various teams to support regulatory and scientific projects.ResponsibilitiesAnalyze real-world datasets to support epidemiologic, scientific, and regulatory projectsBuild, validate, and maintain SAS programs for analysis datasets and study outputsTransform raw real-world data sources—including EMR, EHR, claims, and registries—into accurate, traceable, analysis-ready datasetsPerform quality control and peer review to ensure programming deliverables are accurate and aligned with study plans and SOPsDocument programming decisions and dataset derivations to support reproducibility and audit readinessReview and validate SAS code and outputs developed by other programmersPartner with cross-functional teams including epidemiology, biostatistics, medical writing, regulatory, and client stakeholdersFollow internal SOPs, FDA RWE guidance, and other applicable regulatory standardsSkillsEducation: BS or MS in statistics, biostatistics, epidemiology, computer science, or a related quantitative fieldExperience: 5+ years of SAS programming experience in life sciences, ideally supporting observational research, epidemiologic studies, or regulatory projects using real-world dataSpecial Skills: Strong understanding of real-world data structures, especially EMR- and EHR-based datasets, as well as claims and registry dataExperience supporting retrospective cohort, natural history, burden of illness, comparative effectiveness, and other epidemiologic study designsStrong programming skills in SAS, with R experience beneficial for data analysis, programming, and statistical workflowsStrong documentation skills, including code annotation, traceability, and reproducibilityExperience with Veeva Vault or similar document management systems is a plusPersonal Characteristics: Collaborative, detail-oriented, and comfortable working across epidemiology, biostatistics, medical writing, and regulatory teamsAble to work independently in a remote environment and manage timelines effectivelyExperience with R for data analysis, programming, or statistical workflows is highly beneficialExperience working with Truveta data or similar EMR-based real-world data sources is highly beneficialBenefits401k matchComprehensive group health, dental, vision benefitsLife insurance/LTDDiscretionary PTOCompany OverviewSlipstream is a trusted technology partner exclusively serving the Life Sciences industry. It was founded in 2020, and is headquartered in Blue Bell, Pennsylvania, USA, with a workforce of 201-500 employees. Its website is https://www.slipstream-it.com.Company H1B SponsorshipSlipstream Life Sciences has a track record of offering H1B sponsorships, with 2 in 2026, 1 in 2025, 7 in 2024, 1 in 2023, 1 in 2022, 4 in 2021. Please note that this does not guarantee sponsorship for this specific role.