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SAS Programmer
Ref No.: 15-04562
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.    

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 highly preferred.   Masters or Bachelors degree preferably in a related field (Statistics, Applied Mathematics, Computer Science, Public Health); 2 to 5 years of practical experience SAS programming or conducting analyses in clinical research environment or related field, or an equivalent combination of education and experience.