Description
The Contract Statistical Programmer will develop, test, validate, document, maintain and execute programs in SAS and may serve as lead programmer as appropriate. Will take primary role in review and validation of SAS programs created by more junior-level programmers. Will ensure that all required documentation is appropriately filled out and approved.Responsibilities will include:
- Program, document, validate and review summary tables, data listings, and graphs for inclusion in clinical reports or presentations in collaboration with project statistician.
- Program analysis datasets, will be responsible for responding to data requests in collaboration with project statistician.
- Develop program specifications and design documents under supervision of project statistician
- Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming, reporting, and review
Required Skills, Experience and Education:
- A minimum of five (5) years of solid SAS programming experience with clinical trial data within the pharmaceutical / biotech / medical device industry required.
- A bachelor's degree, preferably in Mathematics, Statistics, Computer Science or related field required.
- A Master's degree in Statistics is preferred.
- Knowledge of Windows operating systems required
- Good oral and written communication skills are essential
Only qualified candidates will be contacted. This is a Staff level role and applicants with less experience will not be considered.