REQUIREMENTS

Candidate will have Phase I - Phase III study experience and at least 2 years of pharmaceutical experience. Candidate will be comfortable with PC SAS version 8.2 and will be responsible for editing and validating programs using SAS macros to generate listings and tables for the study reports and NDA submissions; data step manipulations for data quality assurance/validation of table, listing and summaries, using SAS to analyze clinical data from CRF's; creating SAS data sets for the purpose of analysis and report writing for clinical trials; generating efficacy and safety reports; creating datasets and generating reports using PROC Report (ODS and HTML), SAS arrays, PROC SQL and Macros, SAS Graph, SAS Stat; and verifying and documenting programs. SAS Internet is a plus.

HOW TO APPLY

Qualified and interested candidates are encouraged to apply to joe.mills[at]asg-inc.com. ASG, Inc, places clinical SAS programmers nationally so let us know if you have an interest in another area.

[Please reference Bioinformatics.Org when responding to this announcement.]