Clinical SAS Programmer

RESPONSIBILITIES

Program for the production of template tables, data tabulations, data listings and figures for inclusion in analysis plans and clinical trial reports.
Analyzing and evaluating clinical data, recognizing inconsistencies and initiating resolution of data problems.
Investigate and evaluate new tools and approaches to programming in clinical trials.
Provide feedback to data management on the development of clinical databases and case report forms.
Interacts with statisticians, data management personnel, project leaders, and sponsors.
Other related task as assigned.

REQUIREMENTS

Bachelor?s or Master?s degree in a related field.
Minimum of 2 to 5 years of SAS Programming experience in a clinical research (CRO) or pharmaceutical setting.
Good understanding of statistical methodology.
Excellent written and verbal English language skills.

HOW TO APPLY

Please forward your resume with your salary requirements to tbrady[at]bradygroupinc.com