Senior SAS Programmer/Analyst (Park Ridge, NJ)

Primary Responsibilities:
-Perform SAS programming to provide data review complex listings/reports to support Data Management function for Oncology trials
-Write SAS tools and develop generic SAS programs for clinical studies
-Develop programs for patient profiles and ad hoc reports for data review to support the clinical teams for Oncology trials
-Program data edit checks as necessary to facilitate Data Management's data cleaning activities
-Design and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage for data review
-Develop and maintain the programs including testing and organizing the SAS datasets, SAS programs and related documentation

Qualifications:
-Must be capable of writing complex generic system related macros
-Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/ SQL
-Min 7-10 years of experience in programming with clinical trial data
-Extensive experience in handling external data, such as lab data, PK, ECG, Tumor, etc.
-Experience with JReview is a plus
-Good understanding of standards specific to clinical trials such as CDISC, SDTM, MedDRA, WHODRUG
-Good understanding of relational databases such as ORACLE, Knowledge of the EDC system, InForm, and underlying data structure is a plus
-Capable of communicating technical concepts
-Good understanding of system development life cycles, GCP, and related regulatory guidelines

Type: Long-term Contract