As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.How you will contribute:Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programmingGenerating and validating analysis datasets/analysis files, and complex tables, listings, and figures ( TLFs)Production and QC / validation programmingGenerating complex ad-hoc reports utilizing raw data and analysis datasetsApplying strong understanding/experience of Efficacy analysisCommunicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiriesPerforming lead duties for assigned clinical study under principle programmers oversightServing as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.Being adaptable and flexible when priorities changeGenerating and validating Non-CDISC transformation datasets and analysis datasetsProficient knowledge with SDTM/ADaM and TLFs. General expertise with FiguresIndividuals should be able to start programs from scratch and have the ability to handle complicated domains and outputs related to the protocol and SAP.They must demonstrate a good understanding of the endpoints and data collection, with the ability to read and write specifications related to the respective implementation guides.R complex macro writing are a plusWhat you offer:Bachelors degree in one of the following fields Statistics, Computer Science, Mathematics, etc.At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical Biotech industry with a bachelors degree or equivalent. At least 6 years of related experience with a masters degree or above.Study lead experience, preferably juggling multiple projects simultaneously.Strong SAS data manipulation, analysis and reporting skills.Strong QC / validation skills.Good ad-hoc reporting skills.Solid ADaM and complex TFL skills.Proficiency in efficacy analysis and survival analysisFamiliarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data.Submissions experience utilizing define.xml and other submission documentsExcellent analytical troubleshooting skills.Ability to provide quality output and deliverables, in adherence with challenging timelines.Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.Please use the below link for job application and quicker response.https://lifelancer.com/jobs/view/37c0ccf8d6e861968c61e0f4f503afad