Must have at least 1 year of prior work experience in each of the following 1. Preparing analysis datasets, tables, listings, and figures for phase I to IV clinical trials and publications, according to specifications; 2. Working with CDISC compliant data sets; 3. Reviewing key study documents including CRFs, SAPs, and clinical study reports; 4. Statistical analysis in drug development processes; 5. Supporting quality control of deliverables related to biostatistics; and 6. Programming in SAS.br br Position permits telecommuting.
Categories: eb3
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