Xyant Technology, established in 1995, is a premier federal systems integrator that provides technical and business solutions in information technology, systems engineering, scientific support and management consulting. 

AWARDS 

Winner of Nationwide Best of the Best Small Business Award from Federal Aviation 

Please send your updated resume to vinoth.xyant@gmail. com

Job Title: SAS Clinical Programmer / Clinical Statistical Programmer

Location: Yonkers, NY

Job Type: Long Term Contract

Direct Client Need

• Responsible for building programs to create SAS datasets from the clinical database, external data sources, and other sources while following the clinical study's protocol or statistical plans.
• Build SAS datasets from clinical database.
• Develop SAS macros, templates and utilities for data cleaning and reporting.
• Utilize SDTM guidelines to build datasets.
• Communicate with an internal team to create deliverables for pharmaceutical and biotechnology clients.
• Implement analyses specified in the protocol or the Statistical Analysis Plan (SAP) while working with the project statistician.
• Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy.
• Write SAS programs to generate tables, listings, and figures and analysis datasets.
• Review CRF annotations and data specifications.
• Work in tandem with Biostatistics and Data Management member on various clinical projects.
• Identify and edit checks per the data validation plan or data management plan.
• Study management reports using SAS.
• Validate the programmed analysis datasets, tables, listing and figures.
• Perform analyses defined in the statistical analysis.
• Prepare clinical and statistical summary reports.
• Communicate with programming and statistics leads.
• Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting.
• Perform quality control on final reports.
• Develop SAS coding and table templates for preparing, processing and analyzing clinical data.
• Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.

• 3 to 5 years of experience in Pharmaceutical or CRO industry experience in clinical reporting and statistical applications systems/sub-systems.
• Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming.
• Proficiency in SAS programming on multiple platforms and operating systems, e.g., Windows, NT, UNIX, VMS, etc. is desirable.
• Able to demonstrate a robust and comprehensive expertise working as a SAS Programmer in the clinical research industry and an understanding of the fundamental principles of programming, program development and review.
• Excellent interpersonal and communication skills.
• Motivation and skills for growth into project management is desirable.

Please send your updated resume with your expected hourly pay rate. I'll reach you to discuss more about this position.

Contact email: vinoth.xyant@gmail. com