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Clinical SAS programmer - Remote


Job Id : 14639

Jobtitle : Clinical SAS Programmer - Remote

Location : Houston, TX

Company Name : IFUSION Inc.

Industry : Information Technology

Salary : $56,000 - $91,000  PER YEAR

Job type : Fulltime

Posted on: 2020-06-26


Required Skills : SAS, Macro, BASE SAS, SASSTAT, SASGRAPH

Benefits : No benefits are available


Job Description:

The position provides Statistical Programming technical leadership and support to team members, delegates tasks appropriately, and tracks progress. The position may also construct estimates of project resource requirements and timelines and routinely briefs management on accomplishments, the status of projects, and any issues. In addition, the position is a designated member of the clinical sub-team in the role of project lead Statistical Programmer for a limited number of studies.

Responsibilities:

  • Effectively designs and codes SAS programs for assigned project(s), consistently meeting objectives of the project.  
  • Codes complex SAS programs for applications designed to analyze and report complex clinical trial data and for electronic submissions of data in CDISC format with minimal instruction or input from supervisor  
  • Provides guidance on the resolution of highly complex clinical trial reporting problems within budget and timeline constraints, while assuring high-quality standards  
  • Performs quality control checks of advanced SAS code and output produced by other Statistical Programmers  
  • Responsible for maintaining an excellent working knowledge of medical data, the design and phases of clinical trials, statistics, relevant regulatory requirements, and the pharmaceutical industry  
  • Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications)  
  • Performs other duties as assigned

Qualifications:

  • M.S. (or equivalent degree) and 5 - 8 years of relevant work experience, or B.S. (or equivalent degree) and 8 - 10 years of relevant work experience
  • Proven record of effective and successful project management tasks and skills  
  • Demonstrates advanced experience with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SASSTAT and SASGRAPH  
  • Demonstrates advanced knowledge of electronic submissions and CDlSC  
  • Displays highly advanced knowledge regarding software validation and system development life cycle concepts  
  • Communicates effectively in verbal presentations and written technical reports to both internal and external customers.

Note:

  • Must have a US Degree

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