Advanced Clinical Data Analyst

2 weeks ago

india beBeeStatistical Full time

Senior Statistical Programmer RoleThis is an exciting opportunity to work as a Senior Statistical Programmer, driving patient treatment innovations in the pharmaceutical industry.Job Description:We are seeking a highly skilled and experienced Senior Statistical Programmer to join our team. The successful candidate will have extensive knowledge of SAS programming and experience working with clinical trial data in the Pharmaceutical & Biotech industry.Key Responsibilities:Data Manipulation and Analysis: Perform data manipulation, analysis, and reporting of clinical trial data using SAS programmingSDTM and ADaM Datasets: Generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and figuresProgramming and QC: Produce and QC/validation programmingAd-hoc Reporting: Generate complex ad-hoc reports using raw dataEfficacy Analysis: Apply strong understanding/experience of efficacy analysisSubmission Documents: Create and review submission documents and eCRTsCommunication: Communicate with internal cross-functional teams and clients for project specifications, status, issues, or inquiriesRequirements:Education: Bachelor's degree in Statistics, Computer Science, Mathematics, etc.SAS Programming Experience: At least 8 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalentStudy Lead Experience: Study lead experience with multiple projects preferredData Manipulation and Analysis Skills: Strong data manipulation, analysis, and reporting skillsClinical Trial Data Knowledge: CDISC SDTM/ADaM standards implementationQC/Validation Skills: QC/validation skillsAd-hoc Reporting Skills: Ad-hoc reporting skillsEfficacy Analysis Proficiency: Efficacy analysis proficiencyDrug Development Life Cycle: Familiarity with drug development life cycle and clinical trials' dataSubmissions Experience: Submissions experience with define.xml and other documents

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