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SAS Programmer - Responsible for developing macros for CTT (Clinical Trial Transparency) project to create xml files for clinical trial results. Perform program documentation on CTT project, detailing uses of macro and macro call examples for accurate historical record and future reference. Use SAS/ SQL to perform merging, interleaving, and concatenating of multiple datasets. Develop, test, modify and debug macro for routine tables/listings/figures. Perform statistical analysis on T test, F test, and Chi-square test, and generate reports using statistical procedures including PROC MEANS, PROC FREQ, PROC UNIVARIATE, PROC GLM, PROC LIFETEST, PROC ANOVA, PROC CANNCORR and PROC REG. Perform SAS programming and data processing for clinical trials. Analyze and load data to database for reporting. Produce tables, listings, and graphs based on study protocols and statisticians’ specifications. Master’s Degree in Computer Science. Knowledge of and/or experience in Java, Java Servlet, JSP, Java Script, HTML, SQL, advanced SAS skills; various data analysis methods including Bayesian Network and Boosting; manipulation of complex data. Resumes to: Clinpharma Clinical Research LLC, attn: Department of Human Resources, 1000 N. West St, Ste. 1200, Wilmington, DE 19801. Job location: Wilmington, DE. Please attach the job description and reference requisition number _19801326__ when you apply.