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.