{"id":4223362,"url":"https://alion.io/job/thermo-fisher-scientific-sr-programmer-analyst-2","title":"Sr Programmer Analyst","company":{"id":7922,"name":"Thermo Fisher Scientific","domain":"thermofisher.com","url":"https://alion.io/company/thermo-fisher-scientific","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":81,"open_postings":371,"ghost_share":0.003,"stale_share":0.741,"repost_share":0.011,"time_to_fill_p50_days":31,"computed_at":"2026-11-15T07:52:55Z"}},"role":"Backend","role_family":"Backend","seniority":"senior","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Bengaluru, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":6,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"SAS","optional":false}],"status":"live","first_seen_at":"2026-11-13T06:36:21Z","employer_posted_date":"2026-11-13","last_verified_at":"2026-11-15T04:58:50Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Work Schedule\nStandard (Mon-Fri)Environmental Conditions\nOfficeJob Description\nSenior Programmer Analyst\nJoin Us as a Senior Programmer Analyst - Make an Impact at the Forefront of Innovation\nThe Senior Programmer Analyst performs advanced bioinformatics programming activities supporting the statistical and computational aspects of clinical research projects.\nAdditionally, the Senior Programmer Analyst:\nWorks independently as a Lead Programmer on moderately complex studies.\nServes as a study team member under the direction of a Lead Programmer on more complex studies.\nProvides training, guidance, and mentoring to junior team members.\nKey Responsibilities\nProgramming & Bioinformatics Activities\nIndependently create, execute, maintain, and validate programs that:Transfer data across multiple data management systems or operating systems.\nCombine data from a variety of sources and structures.\nGenerate and store summary data from multiple sources.\nGenerate reports or combine multiple databases.\nValidate programs that generate listings, tables, and figures using SAS.\n\nStudy Leadership & Project Management\nAct as the Lead Programmer on selected studies of moderate complexity.\nCollaborate directly with project team leaders and client representatives.\nAssess and develop project goals and timelines.\nAssume leadership responsibilities as a contributing member of multidisciplinary clinical trial project teams.\nCommunicate proactively with cross-functional team members to ensure project success.\nAssignment & Quality Management\nManage and document assignments to meet project timelines and quality expectations.\nEnsure compliance with relevant contractual obligations and project requirements.\nPerform quality control reviews of statistical programming deliverables.\nTraining & Development\nContinuously enhance expertise in programming technologies, clinical trials, and the pharmaceutical industry.\nTrain, mentor, and guide junior programmers.\nSupport knowledge sharing within the team.\nDepartmental & Strategic Support\nSupport departmental initiatives and infrastructure by:Representing the company at industry conferences.\nPresenting at internal department meetings.\nAssisting in the development of training materials.\nContributing to departmental documents, policies, SOPs, and working practice documents.\nSupporting proposal and bid activities as requested.\n\nEducation & Experience Requirements\nRequired Qualifications\nMaster's Degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field with a minimum of 6 years of relevant experience\nOR\nBachelor's Degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field (or an equivalent relevant academic/vocational qualification) with a minimum of 6 years of relevant experience.\nRelevant experience should demonstrate the knowledge, skills, and abilities required to perform advanced statistical programming, bioinformatics programming, and clinical trial support responsibilities. 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