Description
Opportunity Snapshot:-Develop, test, validate, document, maintain and execute programs in SAS.
-Prepare, document, and review data listings, summary tables, and graphs for inclusion in clinical reports or presentations.
-Prepare analysis datasets for use by statisticians.
-Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming, reporting, and review.
-Respond to data requests from company team members.
-Develop program specification and design documents under supervision of project statistician.
-Share programming expertise with more junior-level programmers.
Requirements:
-Bachelor's degree in Mathematics, Statistics, or Computer Science. A Master's degree in Statistics is preferred and may be considered to offset minimum experience requirement
- 4+ years SAS programming in a clinical trial setting
-Must have recent experience working on clinical trial data
-Knowledge of Windows operating systems required
-Great oral and written communication skills are essential
-Recent experience in Medical Device, Pharma or Biotech industry required
-No remote work available, position is strictly on-site in Irvine, CA
To find out more about Real please visit www.realstaffing.com