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Sr Clinical Programmer
Ref No.: 18-04631
Location: South San Francisco, California
Sr Clinical Programmer – Clinical Data Management

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 trials.

Duties:
  • 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