Job Opportunity: Biostatistician

We are seeking a detail-oriented and experienced biostatistician to support statistical analyses for clinical research studies. This role involves developing and validating SAS programs, preparing statistical documentation, and ensuring compliance with regulatory standards such as CDISC.
Key Responsibilities:

• Develop, Validate, and Maintain SAS Programs: Generate analysis datasets, tables, listings, and figures (TLFs) as per statistical analysis plans.
• Design and Verify Randomization Codes: Ensure clinical trial integrity by designing and verifying randomization codes.
• Prepare Statistical Sections of Protocols: Include sample size calculations and annotated shell data displays in statistical sections of protocols.
• Provide Specifications for Data Structure and Content: Provide specifications for the structure, content, and algorithms of status and analysis datasets.
• Perform Quality Control (QC) of Data Displays and Datasets: Ensure accuracy and compliance with CDISC standards (SDTM, ADaM).
• Conduct Independent Validation of Datasets: Validate datasets created by other programmers or statisticians.
• Maintain Project Documentation: Maintain project documentation including protocols, annotated CRFs, SAPs, and programming/QC records.
• Organize and Manage Electronic Project Directories: Ensure accessibility and version control of electronic project directories.
• Mentor Junior Programmers: Mentor junior programmers and provide training on SAS programming and clinical data standards.

---