CLINICAL SAS PROGRAMMER

ACL Digital

King of Prussia, PA, United States

11 days ago

Role details

Contract type

Permanent contract

Employment type

Full-time (> 32 hours)

Experience level

Expert

Experience required

2 years minimum

Working hours

Regular working hours

Job source

Clean Code Principles Clinical Data Repository Data Files SAS (Software) Utility Software Extensible Markup Language (XML) Information Technology

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.
Assist 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.

Master’s degree Statistics, Computer Science, Engineering or related discipline
24 months experience, Clinical Data Interchange Standards Consortium (CDISC), Clinical Study Publications, Computer Science, Data Sets, Pinnacle, Procedure Development, Quality Control, Regulatory Requirements, Statistical Analysis System (SAS), Statistics, XML (EXtensible Markup Language)