Job Description

Key Responsibilities:

  • Provide technical leadership in SAS programs and applications designed to analyze and report complex clinical trial data in Tables, Listings, and Figures , and for electronic submissions of SDTM, ADaM datasets in CDlSC format, with minimal instruction or input from supervisor

  • Provide technical leadership to create, review, and approve documentation required to support data analysis, reporting, and CDlSC data submission

  • Ensure compliance with company SOP'S and FDA/ICH/GCP regulations

  • Perform quality control checks of advanced SAS code for datasets and output produced by other statistical programmers

  • Review, maintain study documents per standard process

  • Program, test, and document global utility programs and tools in accordance with standards and validation procedures

  • Conduct briefings an...

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