" \u003cdiv class=\"ja-job-details\"\u003e \u003ch2 class=\"title\"\u003eSenior /Principal Statistical Programmer\u003c/h2\u003e \u003cdiv class=\"meta\"\u003e \u003cul class=\"classifications\"\u003e \u003cli data-id=\"23519\"\u003e Biometrics \u003c/li\u003e \u003cli data-id=\"23520\"\u003e Senior Statistical Programmer \u003c/li\u003e \u003cli data-id=\"23521\"\u003e India \u003c/li\u003e \u003cli data-id=\"23522\"\u003e Permanent / Full Time \u003c/li\u003e \u003c/ul\u003e \u003cp class=\"date-posted\"\u003e 16/10/2026 \u003c/p\u003e \u003c/div\u003e \u003cdiv class=\"description\"\u003e \u003cstrong\u003eWho are we?\u0026nbsp;\u003c/strong\u003e\u003cbr\u003e \u0026nbsp;\u0026nbsp;\u003cbr\u003e We\u0026rsquo;re\u0026nbsp;Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area\u0026nbsp;with our founding roots dating back to the 1980\u0026rsquo;s. If you\u0026nbsp;already\u0026nbsp;work in this\u0026nbsp;industry\u0026nbsp;you\u0026rsquo;ll\u0026nbsp;know that we are experts in our field.\u0026nbsp;\u0026nbsp;\u003cbr\u003e \u0026nbsp;\u0026nbsp;\u003cbr\u003e \u003cstrong\u003eWhy should you join Avance Clinical?\u0026nbsp;\u003c/strong\u003e\u003cbr\u003e We appreciate that our most important asset is our people. We offer a fun, friendly work\u0026nbsp;environment\u0026nbsp;and a culture that values honesty and respect.\u0026nbsp;We have\u0026nbsp;a strong sense\u0026nbsp;of team. We genuinely appreciate\u0026nbsp;each individual\u0026nbsp;but recognise the collective\u0026nbsp;when\u0026nbsp;achieving success.\u0026nbsp;\u0026nbsp;\u003cbr\u003e We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.\u0026nbsp;\u003cbr\u003e \u0026nbsp;\u0026nbsp;\u003cbr\u003e \u003cstrong\u003eBroad Purpose\u003c/strong\u003e\u003cbr\u003e This is a full-time on-site/hybrid \u0026nbsp;role for a Statistical Programmer based in Bengaluru. The Senior/Principal Statistical Programmer will be responsible for developing, validating, and maintaining statistical programming outputs including datasets, listings, tables, and graphs for clinical trials. This role involves collaborating with biostatisticians and data management teams, programming complex algorithms, writing macros, managing datasets, and ensuring compliance with regulatory requirements.\u003cbr\u003e \u0026nbsp;\u0026nbsp;\u003cbr\u003e \u003cstrong\u003eCore Responsibilities \u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003ePreparation of listings, tables and figures for clinical study reports.\u003c/li\u003e \u003cli\u003eCreation of primary and QC SAS programs for CDISC datasets and associated documentation.\u003c/li\u003e \u003cli\u003eAssists with the preparation of statistical analysis plans (including preparation/review of listing, table and figure shells) and randomization schedules.\u003c/li\u003e \u003cli\u003eLiaising with Data Management team and bioanalytical laboratories regarding data transfer.\u003c/li\u003e \u003cli\u003eManagement of project specific programming tasks and deliverables (including maintenance of planning documents and regular communication with internal stakeholders) to ensure project team will provide statistical programming deliverables according to project timelines.\u003c/li\u003e \u003cli\u003eMaintain and coordinate CDISC standards, ensure maximum reuse of applied standards and involvement in ongoing process improvement initiatives\u003c/li\u003e \u003cli\u003eStay current with the evolution of all CDISC standards and be involved in creation and maintenance of process documentation\u003c/li\u003e \u003cli\u003eContribute to the development and improvement of Avance procedures related to statistical programming.\u003c/li\u003e \u003cli\u003eOther duties as directed by Line Management or delegate.\u003c/li\u003e \u003c/ul\u003e \u0026nbsp;\u0026nbsp;\u003cbr\u003e \u003cstrong\u003eQualifications, Skills and Experience\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eOrdinary degree in the appropriate discipline or appropriate industry experience.\u003c/li\u003e \u003cli\u003eMinimum 8 years\u0026rsquo; experience in statistical programming in pharmaceutical / health research.\u003c/li\u003e \u003cli\u003eMinimum 2-3 years in Oncology Therapeutics Area Programming\u003c/li\u003e \u003cli\u003eStrong CDISC knowledge and SDTM conversion experience\u003c/li\u003e \u003cli\u003eExperience with development, documentation, and testing of analysis data and programming code to meet regulatory and company standards\u003c/li\u003e \u003c/ul\u003e \u003c/div\u003e \u003cdiv class=\"apply\"\u003e \u003ca class=\"back-link\" href=\"#\" title=\"Back to search results\"\u003eBack to search results\u003c/a\u003e \u003cinput type=\"button\" class=\"ja-button\" data-job-id=\"916422\" value=\"Apply Now\" title=\"Apply Now\" /\u003e \u003c/div\u003e \u003c/div\u003e "