to early and late phase clinical trials. Excellent skills in SAS programming and statistical reporting. Knowledge of CDISC...Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment... and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical...