Senior Statistical Programmer
2 weeks ago
scientific rigor
to reveal the full promise inherent in data.We nurture
intellectual curiosity
and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.We believe in
collaboration
and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.We prize
innovation
and seek intelligent solutions using leading-edge technology.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 TLF’s. 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:Bachelor’s 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 bachelor’s degree or equivalent. At least 6 years of related experience with a master’s 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.Why Cytel?Our collaborative working environment encourages innovation and rewards results, and we are proud to have one of the lowest turnover rates in the industry.In addition to a competitive compensation, we offer an excellent benefit’s package, annual bonus incentive, promote work-life balance, and the opportunity to grow with usWork with respected experts and thought leaders in the fields of biostatistics and statistical programming.
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Senior Statistical Programmer
3 weeks ago
Delhi, India Cytel Software Corporation Full timeCytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services.At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where...
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Senior statistical programmer
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Delhi, India Cytel Full timeCytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where...
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Statistical Programmer
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Delhi, Delhi, India Cytel Full timeAt Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come together to advance the state of clinical development.Working under the direction of Senior Statistical Programmer/Team Lead,...
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1 month ago
Delhi, India Dataceria Full timeStatistical senior programmer Ideal Candidate Should Posses the below Skills1) Clinical SAS Programming2) R Programming3) SDTM, ADAM and TFLs4) SDISC standards5) PK/PD experience6) Knowledge in respiratory therapeutic area would be added advantage.Field-PK/PD experiencePreferred candidate profile - 5 to 8 years experience in Clinical SAS...
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Statistical Programmer
6 days ago
Delhi, Delhi, India Cytel Software Corporation Full timeWorking under the direction of Senior Statistical Programmer/Team Lead, theStatistical Programmerconducts programming activities for a trial, early-phase project, indication, or publication activities.Responsibilities include:Read and understand the program specifications document.Prepare SAS analysis datasets, tables, listings, and figures as per...
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