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.
Must have experience with SDTM & ADaM.
Must have at least 7 years of pharma industry.
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