{"schemaVersion":"jobsearcher.job.v1","id":"e7ee4a8c8e88d123e1b24dc4","url":"https://jobsearcher.com/jobs/e7ee4a8c8e88d123e1b24dc4","canonicalUrl":"https://jobsearcher.com/jobs/e7ee4a8c8e88d123e1b24dc4","title":"Senior Statistical Programmer - Remote (US)","description":"Senior Statistical Programmer - Remote (US) Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMSis an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains an industry‐leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.Job Specific SkillsMastery and training on generating tables, listings, and graphs from clinical trial databases using SASUtilizes System Development Life Cycle (SDLC) for programming deliverablesAdvanced user in SAS programming, SAS Base, and SAS MacrosAdvanced knowledge of E‐Submission Standards, Guidelines and RegulationsMastery and training on SDTM standards including ability to write specificationsAdvanced knowledge of ADaM standards including supporting specification writingProficient with MS Office applicationsAdvanced knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirementsAdvanced experience with pooling of data sets for submissionsAdvanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSPLead study or small programming project teamsJob RequirementsMasters required for all Statistics rolesMinimum of 5 years' experience in Statistical Programming or similar field requiredExpert knowledge of scientific principles and conceptsReputation as emerging leader in field with sustained performance and accomplishmentProficiency with MS Office applicationsHands‐on experience with clinical trial and pharmaceutical development preferredGood communication skills and willingness to work with others to clearly understand needs and solve problemsExcellent problem‐solving skillsGood organizational and communication skillsFamiliarity with current ISO 9001 and ISO 27001 standards preferredFamiliarity with 21 CFR Part 11, FDA, and GCP requirementsBasic understanding of CROs and scientific & clinical data/terminology, and the drug development processSeniority LevelMid‐Senior levelEmployment TypeFull‐timeJob FunctionSales, General Business, and EducationIndustriesWireless Services, Telecommunications, and Communications Equipment Manufacturing#J-18808-Ljbffr","company":"Mms","rawCompany":"mms","isRemote":true,"isActive":false,"createdAt":"2026-05-12T08:45:24.347Z","occupations":[{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"43-9111.00","title":"Statistical Assistants","slug":"statistical-assistants"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541910","title":"Marketing Research and Public Opinion Polling","slug":"marketing-research-and-public-opinion-polling"},{"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":"Senior Statistical Programmer - Remote (US)","description":"Senior Statistical Programmer - Remote (US) Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMSis an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains an industry‐leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.Job Specific SkillsMastery and training on generating tables, listings, and graphs from clinical trial databases using SASUtilizes System Development Life Cycle (SDLC) for programming deliverablesAdvanced user in SAS programming, SAS Base, and SAS MacrosAdvanced knowledge of E‐Submission Standards, Guidelines and RegulationsMastery and training on SDTM standards including ability to write specificationsAdvanced knowledge of ADaM standards including supporting specification writingProficient with MS Office applicationsAdvanced knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirementsAdvanced experience with pooling of data sets for submissionsAdvanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSPLead study or small programming project teamsJob RequirementsMasters required for all Statistics rolesMinimum of 5 years' experience in Statistical Programming or similar field requiredExpert knowledge of scientific principles and conceptsReputation as emerging leader in field with sustained performance and accomplishmentProficiency with MS Office applicationsHands‐on experience with clinical trial and pharmaceutical development preferredGood communication skills and willingness to work with others to clearly understand needs and solve problemsExcellent problem‐solving skillsGood organizational and communication skillsFamiliarity with current ISO 9001 and ISO 27001 standards preferredFamiliarity with 21 CFR Part 11, FDA, and GCP requirementsBasic understanding of CROs and scientific & clinical data/terminology, and the drug development processSeniority LevelMid‐Senior levelEmployment TypeFull‐timeJob FunctionSales, General Business, and EducationIndustriesWireless Services, Telecommunications, and Communications Equipment Manufacturing#J-18808-Ljbffr","datePosted":"2026-05-12T08:45:24.347Z","dateModified":"2026-05-12T08:45:24.347Z","hiringOrganization":{"@type":"Organization","name":"Mms","sameAs":"https://jobsearcher.com"},"jobLocationType":"TELECOMMUTE","applicantLocationRequirements":{"@type":"Country","name":"US"},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e7ee4a8c8e88d123e1b24dc4"},"url":"https://jobsearcher.com/jobs/e7ee4a8c8e88d123e1b24dc4"}}