{"id":2736991,"url":"https://alion.io/job/kyverna-therapeutics-statistical-programmer-consultant","title":"Statistical Programmer Consultant","company":{"id":3959,"name":"Kyverna Therapeutics","domain":"kyvernatx.com","url":"https://alion.io/company/kyverna-therapeutics","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Lever","truth_index":null},"role":"Early Careers","role_family":"Early Careers","seniority":"senior","employment_type":null,"work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":[],"countries":[],"hiring_countries":["US"],"hiring_countries_total":1,"salary":{"min":80,"max":100,"currency":"USD","period":"hour","gross":null,"usd_annual":200000},"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"SAS","optional":false},{"name":"SQL","optional":false}],"status":"live","first_seen_at":"2026-10-16T17:12:45Z","employer_posted_date":"2026-10-16","last_verified_at":"2026-10-17T13:09:09Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.\nTitle: Statistical Programmer Consultant\nReports to: Director, Statistical Programming\nLocation: Remote (West coast hours preferred)\nDuration: 6 months\nHours: 40/hrs per week\nHourly rate: $80-100/hr\nSummary\nWe are seeking a Statistical Programmer Consultant to independently lead statistical programming activities and provide technical support for assigned clinical trial(s). This role combines study-level leadership, strong knowledge of clinical trial data, direct programming expertise to generate datasets, tables, listings, figures, and regulatory submission deliverables.\nResponsibilities\nAct as the lead programmer for assigned clinical trial(s), and work closely with study statistician, clinical data management, and other functions within the study team to provide expert input and statistical programming support.\nLead the strategic design, creation, mapping, and validation of comprehensive SDTM and ADaM datasets, ensuring flawless execution of data traceabilities.\nPerform statistical analysis, program and validate Tables, Listings, and Figures (TLFs) using SAS to support Clinical Study Reports (CSRs), Development Safety Update Report (DSUR), ad-hoc requests, and publications.\nReview and ensure high quality of CDISC packages including aCRF, SDTM/ADaM datasets, Pinnacle 21 reports, cSDRG/ADRG, and define XML meeting CDISC standards and regulatory requirements as part of eCTD submission.\nPerform other duties as assigned.\nQualifications\nBachelor’s, Master’s in Statistics, Biostatistics, Computer Science, Mathematics, or a highly related Scientific discipline.\n8+ years of statistical programing experience within a bio/pharma company, or clinical research organization (CRO).\nAdvanced proficiency in SAS (including complicated data steps, Macro language, and commonly used analysis procedures (e.g., PROC FREQ, PROC REPORT, PROC SQL, and PROC MIXED).\nComprehensive understanding of CDISC standards and experience generating regulatory package artifacts like define.xml and Reviewer's Guides (cSDRG, ADRG).\nStrong communication, analytical, and problem-solving skills, with excellent time management and the ability to independently manage multiple high-priority projects in a fast-paced environment.\nExcellent interpersonal skills and the ability to collaborate effectively as part of a cross-functional team.\nDemonstrated ability to 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