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.
Responsibilities & Duties
- Generate randomization schedules.
- 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.
Qualifications & Skills Technical Skills: OS: Linux, Windows
Web: LAMP stack, microservices, REST API, etc.
Human Skills Leadership
Communication
Work / Experience
Experience in analysis, design, coding, and testing