Full-time jobs in Raleigh, NC

About the role

1. Collaborates in the process of protocol development by choosing an appropriate study design, including statistical methodologies, calculating necessary sample size to achieve a pre-specified power, and writing the statistical section of the protocol. Sample size calculations may require some literature search to ensure that the study assumptions are correct. 2. Writes and reviews Statistical Analysis Plans (SAPs) based on the protocol, including development of well presented mock-up displays for tables, listings, and figures. Collaborates with sponsor. 3. Directs the activities of other Biostatistics personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other statisticians in the department. 4. Participates in project teams as Biostatistics representative, interfacing as necessary with other departmental project team representatives. 5. Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings.

What you'll bring

• MS or PhD in Biostatistics or related field.
• Moderate experience in clinical trials or equivalent combination of education and experience.
• Experience in SAS programming.
• Excellent knowledge of statistical theory including
• experimental design, categorical data analysis, analysis of variance (covariance), survival analysis, and nonparametric methods.
• Effective written and verbal communication skills.
• Ability to apply knowledge of basic
• statistical design, analysis, ICH guidelines, and programming techniques utilized in clinical research and to effectively communicate statistical concepts.
• Ability to read, write, speak, and understand English.