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Job Description
📋 Description Leads the statistical programming activities for studies with lower complexity Develop SAS programs for ADaM data sets following CDISC standards Develop SAS programs for Tables, Listings and Figures; validate outputs Create specifications for ADaM data structures for studies and integrated data Create documentation for regulatory filings including reviewers guides and data definitions Lead development of standard SAS Macros and contribute to SOPs 🎯 Requirements Bachelor's in Statistics, Computer Science or related field 8+ years quantitative analysis (6+ with Masters) SAS programming experience; lead programming for clinical trials ADaM data sets creation and CDISC standards; familiarity with regulatory filings R programming experience; Oncology experience preferred Ability to communicate clearly and mentor staff 🎁 Benefits Paid time off (vacation, holidays, sick) Medical/dental/vision insurance and 401(k) to eligible employees Eligible to participate in short-term incentive programs
