Responsibilities

• Lead statistical activities for clinical trials and data analyses, including study design, statistical analysis plan development, and statistical analysis.
• Provide statistical expertise to cross‑functional teams, including clinical operations, data management, and regulatory affairs.
• Ensure the quality and accuracy of statistical deliverables, including statistical reports, tables, listings, and graphs.
• Participate in the development and review of clinical study protocols and case report forms (CRFs) to ensure appropriate statistical analysis.
• Develop and maintain SAS programs for statistical analysis in accordance with standard operating procedures (SOPs), good programming practices, and regulatory guidelines.
• Keep up to date with regulatory guidelines and industry standards related to biostatistics and ensure compliance with these guidelines.
• Participate in the development and maintenan...