Description
Duties:The Statistical Programmer Analyst applies intermediate to senior level programming techniques and helps plan, design, develop, implement, and maintain software for the monitoring, reporting, and analysis of clinical trials. Prepares and distributes summarized information to the study team. Reviews and implements data warehouse and database designs.
Skills:
Capable of implementing these deliverables in clear, efficient SAS code for the purposes of data analysis and reporting. Computer Systems:UNIX, edit/execute makefile, Oracle Clinical or equivalent clinical DM system, and relational database theory. Desktop: Basic Word/Excel/PowerPoint. Regulatory: Basic knowledge of FDA/ICH guidelines and the software development life cycle. Experience dealing with FDA/regulatory requests. Clinical Trials: 6+ years of pharma/biotech prefered. Understands Biometrics roles in clinical trials. Understands data flow. Communication: Capable of clear and timely written/verbal communication and listening/understanding with Implementation Team (IT), SP department. Effectively expresses concepts and positions in individual and informal group situations. Presents ideas in an organized and concise manner.
Education:
Education: Bachelors. SAS: 4+ years (2+ with a Masters); SAS/BASE, macros, PROC SQL, advanced data step, PROC REPORT, PROC TABULATE, and basic SAS/GRAPH. Statistics:Knowledge and application of p-values, confidence intervals, linear regression analysis, basic general linear models, frequencies, survival analysis, non-parametric analysis.
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