Statistical Analyst
Vanda is seeking a Statistical Analyst who will primarily be responsible for the development, validation, maintenance, documentation of programming codes used in the analysis of clinical trials. The programmer will work interactively with biostatistics, data management, clinical and regulatory personnel and other departments as appropriate.
Primary Responsibilities
- Provide SAS statistical programming support for multiple clinical research projects or regulatory submissions
- Produce and/or validate SDTM/ADaM datasets, analyses, tabulations, graphics and listings of clinical trials data
- Contribute to on-going quality improvement efforts within the project
Requirements
- MS degree or higher degree in statistics, mathematics, or a related quantitative field with at least 3 years of industry related experience for Sr. statistical analyst and 5 years of industry related experience as a Manager, statistical analyst.
- Expertise in the production and review of datasets, analyses, tabulations, graphics and listings from clinical trial data
- Strong experience in Base SAS, SAS/STAT, SAS Macro language and SAS SQL; SAS/GRAPH (a plus)
- Proficient with development, documentation, and testing of analysis data and programming code to meet regulatory and company standards
- An excellent knowledge of CDISCs, such as Study Data Tabulation Models (SDTM)
- Good organizational and communication skills, the ability to work in a collaborative environment, and a desire to improve skills are essential
Vanda Pharmaceuticals offers a competitive compensation package with excellent benefits and a 401(k) matching program. Vanda is an equal opportunity employer, committed to the hiring, advancement and fair treatment of individuals without regard to race, color, religion, sex, sexual preference, age, national origin, ethnicity, disability, or any other protected status designated by law.