Applicants with any suitable combination of education, training or experience are acceptable.br br Experience in item H.10 must include SAS programming for clinical data analysis in pharmaceutical, biotech or CRO environment, implementing statistical programming procedures in SAS to generate SDTMADAM datasets, Tables, Figures and Listings, defining derived variables and missing data handling procedures, creating SDTM and ADAM specifications in compliance with CDISC standards and MACRO program to improve deliverable efficiency, preparing esubmission package aCRF, define.pdf, define.xml, Analysis Data Reviewers Guide, Study Data Reviewers Guide for Clinical Data to submit to FDA, interpreting statistical results and presenting study findings.br br Proficiency in SAS, R, Python, SQL and CDISC standards.br br National Telecommuting.
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