SAS Clinical Programmer
No 3rd party agencies! Direct W2 employees only! Job Summary The Sr Clinical Programmer works in concert with study implementation teams to develop and document standard specification documents for clinical data received by Clinical Data Management (CDM).
CPs model and transform data into CDISC standard data listings and datasets, and also develop data quality reports to assist in data review of clinical trial Dutie Develop and document standard specifications for tabulation of clinical trial data; write programs to process, transform, and report in CDISC standard format (SDTM) for analysis Perform QC and unit testing of SDTM domains Design, develop, implement, and maintain standard reports in Spotfire for data cleaning purposes Customize standard report templates to produce study-specific data quality reports Create patient profile reports Collaborate with internal team and stakeholders to ensure deliverables meet timelines Skills Deep knowledge of Base SAS programming Minimum 5 years CDISC SDTM experience Experience extracting clinical data and developing reports Experience working on a Unix-based platform Previous Genentech experience in clinical or statistical programming a plus Biostatistics, statistical design and analysis experience a plus Multi-tasking and verbal and written communication skills essential - Ability to work well with others Desirable Participation in a regulatory filing Experience in relational database language such as SQL Knowledge of other programming languages such as R, Python, Javascript Qualifications BS or higher in statistical analysis, math, computer science, or equivalent degree and/or experience, and 5-8 years' experience programming SAS in the life sciences industry .
Estimated Salary: $20 to $28 per hour based on qualifications.
CPs model and transform data into CDISC standard data listings and datasets, and also develop data quality reports to assist in data review of clinical trial Dutie Develop and document standard specifications for tabulation of clinical trial data; write programs to process, transform, and report in CDISC standard format (SDTM) for analysis Perform QC and unit testing of SDTM domains Design, develop, implement, and maintain standard reports in Spotfire for data cleaning purposes Customize standard report templates to produce study-specific data quality reports Create patient profile reports Collaborate with internal team and stakeholders to ensure deliverables meet timelines Skills Deep knowledge of Base SAS programming Minimum 5 years CDISC SDTM experience Experience extracting clinical data and developing reports Experience working on a Unix-based platform Previous Genentech experience in clinical or statistical programming a plus Biostatistics, statistical design and analysis experience a plus Multi-tasking and verbal and written communication skills essential - Ability to work well with others Desirable Participation in a regulatory filing Experience in relational database language such as SQL Knowledge of other programming languages such as R, Python, Javascript Qualifications BS or higher in statistical analysis, math, computer science, or equivalent degree and/or experience, and 5-8 years' experience programming SAS in the life sciences industry .
Estimated Salary: $20 to $28 per hour based on qualifications.
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