Clinical SAS Programmer - Hopewell, NJ

New Contracts Opportunity!!
Sr. Clinical SAS Programmer
12 month contract to Ext./Hire
Large Pharmaceutical Company
Central New Jersey

Job Responsibilites:
You will be working within a team of 7-8 people in the Oncology space working on multiple studies at the same time.

The individual will be responsible for the following activities:

-Generate data listings, tables and figures (TFL) from clinical data, using SAS or other statistical software
-Create SAS tools to output TFL directly into clinical study reports
-Review clinical protocols, SAP and case report forms
-Create SAS tools to extract data from various sources
-Merge and/or restructure data to create derived analysis datasets, data warehouse, ISS, ISE, CRTS, in support of regulatory submissions
-Provide programming support to in-house and externally hosted electronic data collection (EDC) systems
-Provide programming support to produce CDISC compliant databases (e.g. STDM, ODM, ADAM) for regulatory submissions
-Supervise and mentor less experienced Statistical Programmers

Job Requirements:

- Bachelor's or preferably Master's degree in Biostatistics, Statistics, Epidemiology, Mathematics, Computer Science, Life Sciences or related field
- 5+ years of programming experience in SAS in a pharmaceutical/CRO
- Excellent experience in high-level efficient SAS programming

Please send resumes to me directly with subject line 'Clinical SAS role'

REFERRALS WELCOME!!

Call or email me if you have any questions at all 212-707-8499

Thanks
Paul DaiTo find out more about Real Staffing please visit www.realstaffing.com