{"id":726196,"url":"https://alion.io/job/clinchoice-senior-statistical-programmer-analyst-ii","title":"Senior Statistical Programmer / Analyst II","company":{"id":672996,"name":"ClinChoice","domain":"clinchoice.com","url":"https://alion.io/company/clinchoice","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":{"grade":"B","score":78,"open_postings":17,"ghost_share":0,"stale_share":0.882,"repost_share":0,"time_to_fill_p50_days":39,"computed_at":"2026-11-08T05:47:12Z"}},"role":"Analytics","role_family":"Analytics","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Pasig, Philippines"],"countries":["PH"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":14500,"max_usd":33000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":3468},"experience_years_min":4,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"C++","optional":false},{"name":"CDISC","optional":false},{"name":"Java","optional":false},{"name":"MATLAB","optional":false},{"name":"Python","optional":false},{"name":"SAS","optional":false},{"name":"SQL","optional":false},{"name":"Good Clinical Practice","optional":true},{"name":"Machine Learning","optional":true}],"status":"live","first_seen_at":"2025-12-17T03:10:23Z","employer_posted_date":"2026-09-29","last_verified_at":"2026-11-08T08:34:03Z","board_verified":true,"closed_at":null,"days_open":326,"trust":{"level":"stale","repost_count":0,"flags":["stale"],"days_open":326},"description":"Responsibilities:\nAnnotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines.\nDevelop SDTM specifications and generate SDTM datasets using SAS.\nDevelop ADaM specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan.\nDevelop Tables, Listings, Graphs, Patient Profile in support of the Clinical Study Report, Posters, Manuscripts.\nDevelop ADaM data, Tables, Listings, Figures for Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE).\nCreate electronic submission package to FDA, e.g., define.xml or define.pdf following FDA guidelines with minimum supervision.\nProficient in analyze information and develop innovative solutions to programming and data analysis challenges; \nSupport the point of contact (POC) of programming with statisticians for statistical input and analysis interpretation\nFollow and reinforce regulatory agency requirements during daily job.\nServe as a programming team lead and contribute to department initiative.\nProvide guidance, mentoring, training for team members and help solve issues from cross-functional teams.\nReview draft and final production deliverables for project to ensure quality and consistency.\nSkills and Qualifications:\n\nBachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology or related scientific disciplines.\nMinimum of 4+ years of clinical programming experience, along with 1+ year of project management and 1+ year of people management experience.\nProven knowledge and training in high level computing languages such as. 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