Associate Director, Statistical Programming

Redwood City, California, United States

USD 229K-269K Mid-level Full Time

@ C...

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Found 23d ago

Tasks

Build and execute SAS programs for data analysis exploratory and post hoc reviews
Create reviewer ready outputs and reviewer guides
Develop SAS macros and tools for repeated program use
Develop specifications for statistical analysis plan and clinical study report
Ensure CDISC compliance and submission readiness for study data packages
Evaluate CDISC electronic data packages for completeness and regulatory compliance
Maintain programming standards for validation repeated use and TMF archival
Manage on time and quality delivery of CRO generated analysis results
Plan execute and validate SAS statistical programming for clinical trial analyses
Review CRO generated case report forms database and data transfer specifications
Validate CRO generated data and analysis results

Perks/Benefits

Skills/Tech-stack

Education

Bachelor of Science | Master of Science

Roles

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Associate Director, Statistical Programming

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