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Sr SAS Programmer
Ref No.: 17-00232
Location: Jacksonville, Florida
Provide statistical programming support for clinical trial data reporting under the general guidance of a biostatistician. Develop SAS programs that generate tables, listings and figures and derived datasets that summarize results for clinical trials. Contribute to the development and implementation of programming and reporting standards. Contribute to the development of a macro library. Work closely with data management to assure data quality and consistency. Provide occasional analytical support under the supervision of a biostatistician. These efforts must meet company objectives and satisfy regulatory GCP and ICH requirements and guidelines
Qualifications and Education Requirements:
Education Level: Bachelor's Degree with a major in Science, Information Technology or equivalent
Years of Experience: 7+years
Skills required for this task include, but are not limited to, expert knowledge of/or the ability to: Strong experience and understanding of SAS/BASE Procedures, experience with the SAS Macro language, basic statistical and mathematical knowledge, ability to effectively communicate with a multi-disciplinary project team, and the ability to work independently and meet deadlines. Attention to detail, quality and accuracy are essential. Experience with CDISC data standards (SDTM and ADaM) is required. Willingness to learn new software tools to accomplish final output