{"schemaVersion":"jobsearcher.job.v1","id":"788e427ff2b712cccde1ad66","url":"https://jobsearcher.com/jobs/788e427ff2b712cccde1ad66","canonicalUrl":"https://jobsearcher.com/jobs/788e427ff2b712cccde1ad66","title":"Statistical Programmer","description":"Statistical Programmer — Fractional Contract | Medical Device / Drug | Remote US 🚀Contract Type: Part-Time Fractional Contract (~20 hrs/week) ⏱️Location: Fully Remote — Open to candidates across the US 🌎Impact: Deliver FDA-facing statistical programming for high-stakes medical device programmes, from anywhere in the US 🎯AboutA leading specialist medical device biostatistics consultancy is growing its bench of expert contract programmers to support an expanding portfolio of FDA-facing clinical programmes. Clients are predominantly PE-backed medical device sponsors in spinal, neurological, and adjacent device therapy areas — companies operating under intense regulatory scrutiny where the quality of statistical work directly shapes regulatory outcomes.This is a senior-only shop. Everyone on the team was hired to do the work — not manage it. If you're a programmer who wants to stay close to meaningful science and work at pace with people who set the standard, this is worth your attention.WhyFractional hours. Exciting and fast-paced work. This role is built for programmers who want flexibility without stepping away from high-quality, impactful clinical programmes. You'll be embedded in active medical device trials from day one, working directly alongside senior FDA-facing biostatisticians — and for those with regulatory ambition, there is a clear and supported pathway to get there.What You'll DoDevelop and deliver SAS and/or R programmes across active medical device clinical trialsBuild and validate datasets, tables, figures, and listings to regulatory-ready standardsCollaborate directly with senior biostatisticians on sponsor-facing deliverablesRespond to time-sensitive requests with pace and precision — FDA timelines are realDevelop regulatory knowledge over time, with mentorship available from senior leadershipRequirementsStrong hands-on SAS and/or R programming experience — active delivery, not oversightBackground in clinical trials or a regulated data environmentMedical device experience is a significant advantage — not an absolute requirementCDISC familiarity is useful but not mandatory — device programmes operate differentlyFully remote capable — responsive, self-directed, and reliable without in-person structureIntrinsically curious, eager to learn, and proactive — this team rewards people who go beyond the briefWhy It's SpecialRemote — work from anywhere in the USFractional and flexible — ~20 hours per week with room to growDirect access to some of the most experienced FDA-facing biostatisticians in the device spaceClear pathway into regulatory science for the right candidateWork on genuinely high-stakes programmes for well-capitalised device sponsorsSenior-only environment — no layers, no noise, just high-quality work","company":"Ipharm Consulting","rawCompany":"ipharm consulting","city":"Denver","state":"CO","isRemote":false,"isActive":false,"createdAt":"2026-08-14T14:27:31.610Z","occupations":[{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Statistical Programmer","description":"Statistical Programmer — Fractional Contract | Medical Device / Drug | Remote US 🚀Contract Type: Part-Time Fractional Contract (~20 hrs/week) ⏱️Location: Fully Remote — Open to candidates across the US 🌎Impact: Deliver FDA-facing statistical programming for high-stakes medical device programmes, from anywhere in the US 🎯AboutA leading specialist medical device biostatistics consultancy is growing its bench of expert contract programmers to support an expanding portfolio of FDA-facing clinical programmes. Clients are predominantly PE-backed medical device sponsors in spinal, neurological, and adjacent device therapy areas — companies operating under intense regulatory scrutiny where the quality of statistical work directly shapes regulatory outcomes.This is a senior-only shop. Everyone on the team was hired to do the work — not manage it. If you're a programmer who wants to stay close to meaningful science and work at pace with people who set the standard, this is worth your attention.WhyFractional hours. Exciting and fast-paced work. This role is built for programmers who want flexibility without stepping away from high-quality, impactful clinical programmes. You'll be embedded in active medical device trials from day one, working directly alongside senior FDA-facing biostatisticians — and for those with regulatory ambition, there is a clear and supported pathway to get there.What You'll DoDevelop and deliver SAS and/or R programmes across active medical device clinical trialsBuild and validate datasets, tables, figures, and listings to regulatory-ready standardsCollaborate directly with senior biostatisticians on sponsor-facing deliverablesRespond to time-sensitive requests with pace and precision — FDA timelines are realDevelop regulatory knowledge over time, with mentorship available from senior leadershipRequirementsStrong hands-on SAS and/or R programming experience — active delivery, not oversightBackground in clinical trials or a regulated data environmentMedical device experience is a significant advantage — not an absolute requirementCDISC familiarity is useful but not mandatory — device programmes operate differentlyFully remote capable — responsive, self-directed, and reliable without in-person structureIntrinsically curious, eager to learn, and proactive — this team rewards people who go beyond the briefWhy It's SpecialRemote — work from anywhere in the USFractional and flexible — ~20 hours per week with room to growDirect access to some of the most experienced FDA-facing biostatisticians in the device spaceClear pathway into regulatory science for the right candidateWork on genuinely high-stakes programmes for well-capitalised device sponsorsSenior-only environment — no layers, no noise, just high-quality work","datePosted":"2026-08-14T14:27:31.610Z","dateModified":"2026-08-14T14:27:31.610Z","hiringOrganization":{"@type":"Organization","name":"Ipharm Consulting","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Denver","addressRegion":"CO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"788e427ff2b712cccde1ad66"},"url":"https://jobsearcher.com/jobs/788e427ff2b712cccde1ad66"}}