Job Description
Provide statistical support for all phases of clinical development. Specific responsibilities include reviewing statistical sections of protocols, writing statistical analysis plans, and developing SAS programs for tables, listings, figures and analysis datasets in accordance with Precision and/or sponsor procedures or study specific guidelines. The individual will generate randomization schedules, assist with statistical methods review of the clinical study protocol, provide input into development of case report forms, and author statistical analysis plans, including development of table, figure and listing shells. They will generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. The individual will also review statistical sections of clinical study reports and work directly with sponsors, project managers, and external vendors on statistics-related project components.
About Precision Medicine Group
Precision Medicine Group is an Equal Opportunity Employer, making employment decisions without regard to race, color, age, religion, sex, sexual orientation, or other characteristics.