SR. CLINICAL SAS PROGRAMMER

ACL Digital

$100K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in Statistics, Computer Science, Engineering, or a related field.
  • Minimum 24 months of relevant professional experience.
  • Proficiency in writing SAS code for datasets and statistical outputs.
  • Experience with CDISC standards and regulatory compliance.
  • Familiarity with validation processes and QC programming practices.

Responsibilities

  • Write SAS code to produce CDISC-compliant datasets.
  • Create statistical analysis outputs for clinical publications.
  • Develop QC SAS programs for datasets, tables, figures, and listings.
  • Revise existing programs for enhancements and corrections.
  • Generate reports and XML documents using Pinnacle 21.
  • Establish programming standards and work instructions.
  • Enhance and validate standardized macros and utility programs.

Benefits

  • Opportunity to work with cutting-edge statistical software.
  • Collaborative work environment emphasizing best practices.
  • Development opportunities in programming and statistics.
  • Participation in clinical research publications and reports.
Full Job Description
DUTIES:
• Proficient to write SAS codes to produce CDISC complaint datasets.
• Create statistical analysis outputs to be used in support of final reports, abstracts, posters, manuscripts, adhocs and other clinical publications.
• Write QC SAS programs for Dataset, Tables, Listings, and Figures following the departmental QC procedures and good programming practices.
• Write programs for ISS, ISE and pooled datasets.
• Revise programs for corrections, enhancements, or system environment changes.
• Proficient to generate Pinnacle 21 reports, Define XML, Define PDFs, and Reviewers Guides. Review Pinnacle 21 report for action needed to fix errors and warnings.
• ssist in establishing standardized programming procedures and work instructions.
• Develop, enhance, evaluate, and validate standardized macros and utility programs.
• Ensure that regulatory requirements are met through validation/compliance activities.
• Use and promote use of established standards, SOP and best practices.

JOB REQUIREMENTS:
  • Master's degree Statistics, Computer Science, Engineering or related discipline
  • 24 months experience
Email resume to: [email protected]

Posted On: 5/21/2026

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