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SAS Programmer

Job in Jersey City, Hudson County, New Jersey, 07390, USA
Listing for: Collabera
Full Time position
Listed on 2026-02-24
Job specializations:
  • IT/Tech
    Data Analyst, Data Scientist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.

Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.

Job Description

Position summary:

The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This position performs statistical programming for clinical studies, integrated summaries, and in support of responses to requests from regulatory authorities.

  • Perform role of primary and validation statistical programmer on all assigned studies, integrated summaries, and in support of responses to questions from regulatory authorities.
  • Create derived data set specifications for all assigned studies and integrated summaries.
  • Create data definition tables for analysis data sets for all assigned studies and integrated summaries.
  • Review statistical analysis plans for all assigned studies and integrated summaries and provide comments to study biostatistician.
  • Review annotated case report forms and provide comments to study designer.
  • Represent Statistical Programming on all assigned project and study teams as needed
Qualifications
  • 3-5 years experience performing statistical programming with SAS in a pharmaceutical or CRO environment
  • Bachelor’s Degree or above in Statistics, Biostatistics, Mathematics, Computer Science, or another related field.
Additional Information

To know more about this opportunity, please contact

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Position Requirements
5+ Years work experience
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