Clinical SAS Programmers

Rang Technologies Inc has openings for Clinical SAS Programmers in Piscataway, NJ, and other unanticipated locations nationwide.Duties:

• Identify project priorities and communicate effectively with the project team and management.
• Interact with Scientists, Biostatisticians, and Data Management teams to gather requirements and specifications for data analysis and report generation.
• Carry out statistical modeling using linear or generalized linear regression and Mix Modeling for prediction and estimation of responses for clinical research data.
• Develop macro applications that process biological and clinical data into in-text reports and searchable listings for medical writers for analysis and presentation.
• Create analytical reports for Integrated Summary of Safety (ISS) / Integrated Summary of Efficacy (ISE) which involve overall safety and efficacy of a drug.
• Write SAS programs to analyze and report data as customized reports (tables, figures, and listings) as per the statistical analysis plans.
• Create and apply data analysis and data mining algorithms for research-based longitudinal data.
• Analyze and validate bioinformatics and laboratory measures using SAS software and statistical methodologies. Confer with database users about data issues, data resolutions, and project timelines.
• Create edit checks procedures, quality control guidance document, and error-checking user manual using efficient statistical procedures and macro facility.
• Participate in compiling and integrating analysis reports for regulatory submissions and scientific publications.
• Conduct quality analyses of data inputs, endpoint derivations, and resulting analyses or predictions.
• Test new tools on biological data, analyze updated macros for pharmacokinetic data, and provide feedback to developers.
• Check source data to verify completeness and accuracy.
• Maintain awareness of emerging computational methods, technologies, and guidance documents provided by Clinical Data Interchange Standards Consortium (CDISC) and make applicable updates to the working documents.
• Document all database changes and maintain various databases as data gets periodically refreshed.
• Create Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) specifications and datasets as per CDISC standards by following controlled terminologies.
• Perform routine system administrative functions and back-up older versions of the database according to standard archival procedures.