Biostatistician

About the Role

We are seeking a highly-motivated Senior Biostatistician to join our team. This position provides statistical support for all phases of clinical development. Specific responsibilities include reviewing statistical sections of protocols, writing statistical analysis plans (SAP), developing SAS programs, and interacting with clients, and participate in FDA meetings as needed.

• Provide sample size calculations.
• Provide input into development of case report forms (CRFs).
• Author statistical analysis plans, including development of table and listing shells.
• Write analysis plans for eCTD submissions.
• Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS.
• Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests.
• Perform quality control for SAS programs and other study documents (e.g., presentations and reports).
• Provide statistical analysis and reports to Data Monitoring Committees (DMCs).
• Review output across programs to ensure consistency.
• Prepare statistical sections of clinical study reports.
• Interact directly with clients.

• Leadership
• Communication

• Experience in analysis, design, coding, and testing
• Experience in leading a cross-functional team