Senior Data Scientist
2 weeks ago
About the RoleWe are seeking a skilled Senior Statistical Programmer to join our team in supporting innovation within pharmaceutical clients. This role involves working fully embedded within a client, dedicated to one or more Phase I-IV clinical trials.Advanced SAS programming skills and proficiency in CDISC standards will be utilized to manipulate, analyze, and report clinical trial data.The role requires generating and validating SDTM and ADaM datasets/analysis files, tables, listings, and figures.Production and QC/validation programming, as well as generating complex ad-hoc reports using raw data, are also key responsibilities.ResponsibilitiesData manipulation, analysis, and reporting of clinical trial data utilizing SAS programming.Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures.Production and QC/validation programming.Generating complex ad-hoc reports utilizing raw data.Efficacy analysis.Submission documents and eCRTs.Communicating with cross-functional teams and clients for project specifications, status, issues, or inquiries.Lead duties when called upon.Serving as a team player, willing to go the extra distance to get results, meet deadlines, etc.QualificationsBachelor's degree in Statistics, Computer Science, Mathematics, etc.At least 8 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry.Study lead experience, preferably juggling multiple projects simultaneously preferred.Strong SAS data manipulation, analysis, and reporting skills.CDCISD SDTM / ADaM standards expertise.QC/validation skills.Ad-hoc reporting skills.Efficacy analysis proficiency.Familiarity with drug development life cycle and clinical trials' data manipulation, analysis, and reporting.Submissions experience utilizing define.xml and other submission documents.Excellent analytical & troubleshooting skills.Ability to provide quality output and deliverables, in adherence with challenging timelines.
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