Clinical SAS Programmer Job at Katalyst Healthcares & Life Sciences, Los Angeles, CA

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  • Katalyst Healthcares & Life Sciences
  • Los Angeles, CA

Job Description

Responsibilities:



  • Author and/or provide input on statistical sections of clinical study documents including protocols, electronic case report forms, randomization plans, data transfer specifications, statistical analysis plans, tables, listings, and figures (TLF) shells, SDTM/ADaM specifications, clinical study reports, and other relevant documents.


  • Drive TLF development and TLF reviews with programming and other relevant team members, determine analysis populations, validate key analysis results, and present final analysis results to key stakeholders.


  • Accountability for 5+ concurrent studies.


  • Represent the Statistics function in study team meetings.


Requirements:



  • Masters or PhD in Statistics.


  • 3-5 years recent/related statistical experience within a pharmaceutical and/or medical device company, or similar organization.


  • Previous experience in Clinical research.


  • Experience with different clinical phases.


  • Knowledge of clinical trial methodology and study design.


  • Study-level statistical expertise.


  • Proficiency in SAS and knowledge of CDISC standards.


  • Strong working knowledge of statistical data analysis and data management principles.


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