Statistical Research Professional
1 week ago
Job Summary:
\Supports all assigned statistical tasks during the lifecycle of clinical trials, from protocol development to Clinical Study Report (CSR). Prepares statistical analysis plans (SAPs), develops tables, listings, and figures (TLFs), and provides programming and biostatistical support for clinical trials. Collaborates with internal teams and sponsors to ensure high-quality deliverables and regulatory compliance.
\Key Responsibilities:
\- Provides comprehensive support across all statistical tasks during the project lifecycle, from protocol to CSR.\
- Prepares Statistical Analysis Plans (SAPs) and develops mock-up displays for tables, listings, and figures.\
- Collaborates with sponsors and coordinates activities of biostatistics and statistical programming personnel.\
- Independently reviews project work produced by other biostatisticians.\
- Creates and reviews programming specifications for analysis datasets, TLFs, and other outputs.\
- Reviews SAS annotated case report forms (CRFs), database designs, and study documentation for completeness and protocol compliance.\
- Conducts verification and quality control of project deliverables to ensure consistency with SAP and specifications.\
- Serves as biostatistics representative on project teams and contributes to internal meetings and discussions.\
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