Clinical SAS Programmer

1 week ago

Fairfield, United States Penfield Search Partners Full time
Job DescriptionJob Description

Contact: Neisha Camacho/Terra Parsons – teamnt@penfieldsearch.com

Role Description:

  • Independently develop/validate programs that generate SDTM and analysis datasets based on ADaM specifications.
  • Prepare/QC ADaM datasets documentation: Define.xml, Reviewer’s Guide and analysis metadata report.
  • Independently develop/validate programs that generate tables and listings specified in the protocol or the Statistical Analysis Plan (SAP)
  • Perform quality control on final reports.
  • Provide QC and validation reports.
  • Support development of technical programming specifications for ADaM standards
  • Communicate with programming and statistics leads, data managers and other team members.
  • Provide project progress updates of programming activities.

Qualifications/Experience:

  • BS/MS in Statistics, Biostatistics, Computer Science, Mathematics or Life Sciences
  • 10+ years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry

Required Skills Include:

  • Strong SAS programming skills required in Windows & UNIX environment with proficiency in SAS/Base, SAS Macros, SAS/Stat
  • Knowledge of working in SAS Grid environment with experience in SAS Enterprise Guide and SAS Studio is a plus.
  • Experience with all clinical phases I, II, III and IV of trials is desirable.
  • Good understanding of standards specific to clinical trials such as CDISC, SDTM, ADaM, MedDRA, WHODRUG
  • Strong problem-solving skills
  • Good organizational and time management skills
  • Excellent communication skills and capability of communicating technical concepts.
  • Excellent organizational skills with demonstrated success to multi-task and deliver viable solutions in a fast-paced environment with changing priorities.

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