US-NC-Durham: SAS Programmer

Date: 07-Dec-2012
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SAS ProgrSAS Programmer • Lead SAS Programmer on one or more project teams: ? Generate the SAS Programming Master Plan for assigned project(s). ? Coordinate project reporting tasks associated with the project. ? Provide input to project timelines, and ensure that project timelines are met for both internal and external clients. ? Ensure that project tasks are completed with superior quality for both internal and external clients. ? Assume responsibility for project SAS Programming budget, and perform monthly time projections for assigned project(s). ? Attend internal team meetings and relevant client team meetings for assigned project(s). ? Coordinate documentation and archival of data, deliverables, and SAS programs for assigned project(s). • CDPS Development: • Statistical analyses, summaries and reports: ? Review and provide comment on summary and analysis plans. ? Develop and/or validate analysis datasets and tables/listings/figures. • Aggregate data checks and other data review activity: ? Review specifications for data management’s planned aggregate data checks. ? Program and/or validate aggregate data checks, data review listings, and any other SAS-based data review reports for project team use. ? Set up project-specific I-Review system, including standard and custom views. • InfoLink and Site Payment systems: ? Write or coordinate development of test data specifications, and coordinate data entry effort. ? Set up standard reports; program and/or validate study-specific criteria for standard repots. ? Develop and/or validate custom reports. • Other reporting development: ? Write or coordinate development of test data specifications, and coordinate data entry effort. ? Develop and/or validate programs to generate reports. • Perform independent code review, and develop test plans, as needed for SAS programming activities. • Perform other duties as assigned.

• Knowledge of clinical research process and methodology.

• Knowledge of programming and validation methods, and software development cycle. • Experience with SAS Base, SAS Stat, SAS Macro, SAS Graph, and ODS as well as strong data step skills. • Knowledge of relational database concepts, experience with Oracle and SQL. • Ability to plan long-range needs while assuming responsibility for daily details with a high degree of accuracy. • Ability to work creatively and independently to carry out assignments of a complex nature. • Ability to communicate and work effectively and cooperatively with other professional staff members. • Excellent organizational and program documentation skills, highly detail-oriented. • Ability to learn new programming languages, new technology, and new tools that will facilitate the clinical trial process.

? High school diploma (or equivalent) with a minimum of four years work experience in programming, including two years SAS programming work experience; or ? Associate degree, with a minimum of three years work experience in programming, including one year SAS programming work experience; or ? BS degree, with a minimum of two years of work experience in programming, including one year SAS programming work experience

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DBA FYI Center
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