Slipstream Life Sciences · 3 weeks ago
Statistical Analytical Programmer
United States
Full-time
Remote
Senior Level
5+ years expSlipstream 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.
ConsultingInformation TechnologyInformation Services
Responsibilities
Analyze real-world datasets to support epidemiologic, scientific, and regulatory projects
Build, validate, and maintain SAS programs for analysis datasets and study outputs
Transform raw real-world data sources—including EMR, EHR, claims, and registries—into accurate, traceable, analysis-ready datasets
Perform quality control and peer review to ensure programming deliverables are accurate and aligned with study plans and SOPs
Document programming decisions and dataset derivations to support reproducibility and audit readiness
Review and validate SAS code and outputs developed by other programmers
Partner with cross-functional teams including epidemiology, biostatistics, medical writing, regulatory, and client stakeholders
Follow internal SOPs, FDA RWE guidance, and other applicable regulatory standards
Qualification
Required
Education: BS or MS in statistics, biostatistics, epidemiology, computer science, or a related quantitative field
Experience: 5+ years of SAS programming experience in life sciences, ideally supporting observational research, epidemiologic studies, or regulatory projects using real-world data
Special Skills: Strong understanding of real-world data structures, especially EMR- and EHR-based datasets, as well as claims and registry data
Experience supporting retrospective cohort, natural history, burden of illness, comparative effectiveness, and other epidemiologic study designs
Strong programming skills in SAS, with R experience beneficial for data analysis, programming, and statistical workflows
Strong documentation skills, including code annotation, traceability, and reproducibility
Experience with Veeva Vault or similar document management systems is a plus
Personal Characteristics: Collaborative, detail-oriented, and comfortable working across epidemiology, biostatistics, medical writing, and regulatory teams
Able to work independently in a remote environment and manage timelines effectively
Preferred
Experience with R for data analysis, programming, or statistical workflows is highly beneficial
Experience working with Truveta data or similar EMR-based real-world data sources is highly beneficial
Benefits
401k match
Comprehensive group health, dental, vision benefits
Life insurance/LTD
Discretionary PTO
Company
Slipstream Life Sciences
Slipstream is a trusted technology partner exclusively serving the Life Sciences industry.
201-500 employees
H1B Sponsorship
Slipstream Life Sciences has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
50%
Represents job field similar to this job
Engineering and Development
Management and Executive
Sales
Customer Service and Support
Trends of Total Sponsorships
*2026 (2)
2025 (1)
2024 (7)
2023 (1)
2022 (1)
2021 (4)
Funding
Current Stage
Growth StageTotal Funding
unknownKey Investors
Denali Growth Partners,GreyLion Capital
2025-08-05Private Equity
Leadership Team
Brandon McKay
Founder/Chief Executive Officer
Recent News
globallegalchronicle.com
2025-08-08
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