Senior Statistical Programmer

Job Description

If you have MS in Statistic and 10+ years experience in SAS programming experience in clinical trials and strong CDISC experience, please apply for interview within 24 hours.  We are interested in H1B/EAD/GreenCard/US Citizen candidates. We are opened for W2 and 1099/corp-to-corp contract. Up to 10 openings available! LONG-TERM contract! Start ASAP! ****PAY RANGE $60 to $100/hr*****

NOTE: We require two or more professional references (supervisor or direct report) prior to phone interview.

 Strong Clinical Statistical programmer - 6-10 openings in NJ

The request below indicates 10+ years SAS programming in Pharma industry. Please note that we will be looking for candidates whose experience is mostly U.S. experience.

The Clinical SAS Programmer is responsible for designing and developing standard software and data structures, developing and executing statistical programs designed to analyze clinical trial information and NDA submissions.

 Additional responsibilities will include:

 Multiple NDA filings which has generated needs for up to 6 strong Statistical Programmers

• Seasoned SAS (Clinical meaning from Pharma/CRO) experience (looking at 8+ years, the more the better)

• Experience working on NDA filings (Big Plus)
• Experience with Complex Efficacy Analysis
• Cardio experience a plus (not required)
• SAS/MACRO experience required
• MS Statistics strongly preferred

Candidates will perform the following job related tasks;

• Review protocols, CRFs, operation manuals and Clinical      Evaluation Committee (CEC) adjudication form as well as databases
• Create SAS programs to generate derived data sets,      tables and listings per specifications, and QC summary tables and maintain      SAS programs for regular updates of deliverables
• Provided programming support to project statistician,      medical director, clinical monitor, and data manager
• Generated and validated data definition tables for NDA      submission

Keywords: Clinical SAS Programmer, Statistical Programmer, Clinical Programmer III, SAS Developer, Statistical Analyst, SAS Programmer, SAS Analyst, Clinical Statistical Programmer, SAS, Statistical, Programming, Clinical SAS, Validation SAS Programmer, Senior SAS Programmer, Lead SAS Programmer, Sr. Statistical Programmer

Please respond directly to Global Employment Solutions, Inc. at rchu@gesnetwork.com  with your resume attached – WORD document.

Job Requirements

Experience & Qualification

• M.S./M.A. in Statistic or Applied Statistic preferred
• 10+ years full time SAS programming experience for      Senior Programmer; experience must be in the pharmaceutical or      biotechnology industry.
• Previous STDM experience as well as ISS, ISE, and TLF.
• Experience working on NDA filings (Big Plus)
• Experience with Complex Efficacy Analysis
• Cardio experience a plus (not required)
• SAS/MACRO experience required

Key to the job:  MS in Statistic with 10+ years pharmaceutical industry SAS programming experience, strong statistical experience, and also strong programming exp in clinical trials and NDA filing.

We appreciate your understanding, in that; we will only be able to respond to those inquiries who meet the stated requirements. To protect our client’s interests, we will not be responding to inquiries that do not contain a CV/Resume. Finally, please include the position ID (rc-Sr. Stat) in the subject line of your correspondence to ensure review. Please forward your credentials in Word format, in confidence, to: rchu@gesnetwork.com  Our clinical recruiter/manager will contact the qualified candidates IMMEDIATELY to set up interviews.