Develop, maintain, and validate high-quality SAS programs for simple to moderate complexity tabulation dataset mapping, analysis datasets and table, figure, and listing (TFL) output.<\/li>\n\n\n\n
Meeting with project managers to determine needs.<\/li>\n\n\n\n
Use appropriate documentation and validation tools to create CDISC compliant tabulation and analysis datasets.<\/li>\n\n\n\n
Develop, maintain, and validate high-quality documentation for tabulation and analysis datasets where appropriate.<\/li>\n\n\n\n
Testing the stability and functionality of the application.<\/li>\n\n\n\n
Provide high quality, timely support that conforms to current company or client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and\/or guidelines on behalf of the client.<\/li>\n\n\n\n
Communicate effectively with Clients and Vendors where appropriate.<\/li>\n\n\n\n
Troubleshooting and fixing bugs.<\/li>\n\n\n\n
Writing documents and providing technical training for End Users.<\/li>\n\n\n\n
Maintaining the security and integrity of the application software.<\/li>\n<\/ul>\n\n\n\n
Requirements:<\/p>\n\n\n\n
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5+ years\u2019 experience as a SAS programmer for a full-service CRO<\/li>\n\n\n\n
Excellent application development skills<\/li>\n\n\n\n
Bachelor\u2019s degree in Statistics, Computer Science, Mathematics, or a related science discipline<\/li>\n\n\n\n
Experience in SAS Base, and good knowledge of SAS graph and SAS Macros<\/li>\n\n\n\n
Extensive knowledge in CDISC, SDTM and ADaM<\/li>\n\n\n\n
(GCP) and International Conference on Harmonization (ICH) guidelines<\/li>\n\n\n\n
Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.<\/li>\n\n\n\n
Experience leading studies<\/li>\n\n\n\n
Excellent communication skills in English, both verbal and written<\/li>\n<\/ul>\n\n\n\n