SAS Programming

Integrated Resources Inc.; Madison (NJ); On-site; USD 80,000 - 120,000; Full time

Job summary

A leading staffing firm seeks a SAS Programmer to lead clinical trial programming efforts in Madison, NJ. The ideal candidate will possess strong SAS expertise and time management skills, ensuring high-quality analyses under sponsor guidelines. This role is essential for producing key reports and working closely with Biostatistics on various projects.

Qualifications

• Graduated with strong expertise in SAS programming.
• Familiarity with Unix platform and CDISC standards preferred.

Responsibilities

• Perform all SAS programming required for clinical trial analysis and reporting.
• Review case report form design and write edit checks from specifications.
• Produce tables, listings, and figures for clinical study reports.

Skills

SAS programming

Time management

Education

Graduated

Tools

Unix

CDISC standards

Job description

A Few Words About Us
Integrated Resources, Inc. is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.

Job Description

Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Leads programming efforts for large, complex studies. Requires strong SAS programming expertise and good time management skills. Reviews case report form (CRF) design, designs and/or reviews database structures, and writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets and executes analyses as specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plans (RAP) under the guidance of the project statistician. Acts as the primary programmer to produce tables, listings, and figures for the clinical study report (CSR). Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses. Familiarity with Unix platform and/or CDISC standards is preferred. Candidate must be able to complete a 1-year assignment. No overtime, no travel required. All work to be performed onsite in Madison.

Qualifications

Graduated

Additional Information

Integrated Resources, Inc.

Contact: 732-429-1912 (W), 732-549-2030 x 232 | Fax: [phone]

LinkedIn: https://www.linkedin.com/pub/kashish-vermani/50/4a5/35a

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