Job Description
Responsibilities:
Develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD.
Guarantee quality of statistical output produced by external provider, to program tools to support data review activities and data visualization, to collaborate on the interpretation and communication of trial results.
Contribute to regulatory submissions, converting data according to regulatory requirements, preparing integrated analyses and related documentation.
Perform post-hoc analysis for exploratory purposes, or to support regulatory requests, to prepare analysis for paper publications.
Support the development of standard operating procedures.
To convert data to CDISC SDTM, following project specifications.
Develop SAS programs to generate analysis datasets (CDISC compliant).
Produce datasets documentation according to CDISC and...
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