SAS Analyst Position Available In Bergen, New Jersey

Perform SAS programming to provide data review complex listings/reports to support Data Management function for Oncology trials. Develop programs for patient profiles and ad hocreports for data review to support the clinical teams for Clinical trials.

Generates and maintains all required documentation including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRF)s,database creation, coding setup, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports. Program data edit checks as necessary tofacilitate Data Management’s data cleaning activities. Design and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the OncologyData Management and other areas of Clinical for data review. Develop and maintain the programs including testing and organizing the SAS datasets, SAS programs and relateddocumentation. Develop and review specifications for data analysis and statistical reports for Phase

III & IV

Studies. Implement and ensure CDISC standards across several clinicalstudies. Design various statistical models such as t’ test, One-way analysis of variance (ANOVA), One-way analysis of co-variance (ANCOVA),Regression analysis and Newman-Keulstests. Develop and review Mock shells (TLF’s), in coordination with statistician. Will also be using SAS/Base, SAS/Macros, SAS/ETL Studio, SAS/QC, SAS/STAT, AERS, CRF’s, SASTransport Files, Medidata RAVE, TDSV, CDISC- SDTM, ADaM, Veeva Vault, Oracle Inform, MS Visio, and MS Project.•Science in Biotechnology, Biomedical, Computer Science or any other related field of study. Any suitable combinations of education, training or experience are acceptable.