CLINICAL PROGRAMMER ANALYST

Major Biotech with a location in South San Francisco is seeking a Clinical Programmer Analyst to join their team.

Compensation is commensurate with experience and education. 

The Clinical Programmer Analyst (CPA) II may serve as the lead programmer for a project or for one or more clinical trials.

Serve as a resource for clinical programming concepts, standards and processes. Maintain a broad perspective on programming issues, activities and deliverables. Collect detailed specifications to direct development of requested listings from appropriate parties. Consult with project teams as to appropriate data review strategies and available options. Advocate use of available data listing standards.Records and maintain work specifications in an accurate and timely manner. Develop SAS code that produces requested outputs with adherence to specifications and department coding conventions. Clearly documents program design choices and other relevant development notes. Stay current with advance development refinement of best practices and coding conventions. Perform code review / program verification of peer programming. Performs data review listing production and publication on schedule.

Requirements:
BA/BS in Computer Science or related field 2 - 4 years of relevant experience  Knowledge of basic software applications (electronic mail, electronic calendar, MS windows, general file server use)  Knowledge of advanced productivity software applications (spreadsheet, presentation, project management) Knowledge of core clinical data management applications (unix, MS Word, web browser, relational database, query tools) Basic knowledge of default SAS views.  Basic OCL background table understanding desirable. Basic understanding of UNIX commands. Solid understanding of Base SAS, Macro Language, Proc Report, and other relevant SAS skills. 

Key Words:  SAS, Data, Analyst, Macro, Clin*, Pharma*, Review, List, Code, SAS, California