Plan, develop, test, manage, and document software additions and changes in accordance with SOPs and in conjunction with biometrics staff and upper management.
Create data sets for data analysis and/or for transfer to external groups as necessary, including potential integration of multiple existing data sets.
Use SAS, or alternative software, to generate documents (e.g. tables, listings, figures, define.doc, define.xml, narratives) that can be submitted to regulatory agencies.
Conduct Quality Control checks on programs and outputs generated by statisticians and other programmers. This involves writing and checking code, as well as output checks and comparisons in accordance with standard operating procedures.
Requirements:
Bachelor's degree in a relevant field is required - a Masters or PhD would be preferable.
Relevant experience in clinical programming.
Advanced SAS programming skills in a clinical data environment.
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