Clinical SAS Programmer

Company: Katalyst Healthcares & Life Sciences
Location: Bayonne
Posted on: January 16, 2023

Job Description:

Responsibilities:

• 
  
• Extract clinical data from the clinical data management system and produce standard and custom reports, primarily in SAS.
  
• Program reports and listings as requested by project team members for ongoing studies. Develop transfer specifications with vendors for external data sources.
  
• Perform consistency checks on data transferred between Incyte and external parties to ensure completeness and accuracy of data contained transfers.
  
• Perform programming to convert raw, clinical trial data to Study Data Tabulation Model (SDTM) format.
  
• Perform Quality Control (QC) on programming work performed by fellow Database Programmers.
  
• Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency.
  
• Qualifications (Minimal acceptable level of education, work experience, and competency)
  
  Requirements:
  
  
  • 
    
  • Bachelor's degree OR certification.
    
  • Minimum of 2 years of clinical SAS programming experience in the pharmaceutical industry.
    
  • Working knowledge of CDISC SDTM mapping/specs/conversion/domains/datasets/eCRF/eCRT
    
  • Package/define.xml development and SDTM data transfer operations on clinical studies.
    
  • Understanding of regulatory requirements relevant to submissions.
    
  • Knowledge of clinical trial study design and electronic data submission requirements.
    
  • Communication and interpersonal skills and the ability to work effectively as part of a team.
    
    
    
    

Keywords: Katalyst Healthcares & Life Sciences, Bayonne , Clinical SAS Programmer, IT / Software / Systems , Bayonne, New Jersey