SAS Developer

Description

JD below Develop and maintain datasets as per the CDISC (SDTM and ADaM) standards; Extract data from various databases;Develop and maintan programs toanalyze the data and procudereports consisting of Tables, Listings and Graphs that are generated from the available databases;Apply Programming Development Life Cycle (PDLC) principles;Develop programs using SAS(Statistical Analysis Software) and SQL;Perform Programming using SAS softwareanalyzing the clinical trial data to produce the outputs for the clinical trial report;Prepare specifications and process flow diagrams, and develop programming code logic flowcharts;Write specifications for the analysis datasets and report (Tables, Listings and Graphs) generation;Prepare reports to assist management in problem analysis, and submit recommendations for solution;Create primary and validation programs;Develop, test, debug and deploy the programs in coordination with other line functions as per standard operating procedures (SOPs);Maintain study documentation;Document and revise system design procedures, test procedures, and programming standards;Analyze user/customer needs and software requirements to determine feasibility of design within time and cost constraints;Create analysis files (datasets), and reports Tables, Listings and Figures;Consult with customers about software design, maintenance, enhancement and customization;Store, retrieve, and manipulate data for analysis and reporting;Expand or modify existing programs for efficiency and reusability; andWork on other ad hoc tasks as assigned.Skills 1 3 years Pharma experience supporting clinical trials Working experience for clinical data; Familiar with trial analysis Familiar with SAS Education Bachelors' Degree or equivalant experience MS BiostatAdvanced SAS Certification requiredcan be verified via the Public Registry of SAS Certified Professionals.