The Statistical Programmer will support the statistical analysis and reporting of data from clinical and nonclinical studies.
ESSENTIAL DUTIES AND RESPONSIBILITIES (include, but are not limited to):
Develop and validate statistical programs to support the analysis and reporting of data from clinical and nonclinical studies in support of all corporate therapeutic program areas.
Have good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.
Demonstrate ability to work in a team environment under the direction of a lead programmer and statistician.
Excellent hands-on programming skills with SAS.
EDUCATION and/or EXPERIENCE:
Bachelor’s degree or equivalent experience with a computer science, mathematics, or statistics major preferred.
In addition, must have a minimum of 2 years of experience in the biopharmaceutical (or CRO) industry as a statistical programmer, and must have excellent SAS programming skills and familiarity with CDISC standards and implementation of those standards.