We are excited to launch this remote opportunity to diverse men and women who are highly experienced in biostatistics with a large, multinational production and services corporation.
Roles and Responsibilities
- Participate in development of the statistical analysis plan (SAP) for clinical studies and execute SAP throughout lifecycle of the study.
- Perform data review and statistical analyses.
- Collaborate in writing statistical sections for integrated reports or/and statistical reports.
- Develop statistical programs as necessary to perform analyses and prepare data displays.
- Participate in developing the case report form (CRF) and of database clinical trial data specifications, including eCRF design, user requirements, edit rules/checks, query logic, and data validations.
- Align with data integrity standards and business ethics requirements.
Requirements
- Master’s degree in Biostatistics
- 3+ years of experience in pharmaceuticals or medical devices
- Strong knowledge of statistical theory, experimental design and clinical trial methodologies, linear and nonlinear modeling, categorical and non-parametric methods, sample size calculations.
- Expertise in SAS is required. Solid knowledge of BASE SAS, SAS/STAT, SAS MACROs, etc.
- Preferred: Familiarity with IVD statistics
Benefits
Competitive compensation that typically has key components including base salary, variable annual incentive compensation based on personal and company performance, and long-term incentive. We also offer comprehensive healthcare plans, savings plans, paid time off, and other benefits.