Associate Principal Scientist, Stat. Programming - A&r Standards, Innovation (hybrid)

Merck Merck · Pharma · PA

This role focuses on developing and validating global programming standards for analysis and reporting in drug and vaccine development within the Biostatistics and Research Decision Sciences department. It requires extensive SAS programming experience in a clinical trial environment and knowledge of CDISC standards.

What you'd actually do

  1. Develop and validate global programming standards for ADaM datasets
  2. Develop and validate global programming standards for efficacy analysis and reporting
  3. Develop and validate global programming standards for safety analysis and reporting
  4. Design and develop complex programming algorithms
  5. Provide technical consultation and analytical support to statistical programmers and statisticians

Skills

Required

  • SAS programming
  • clinical trial programming
  • data steps
  • procedures
  • SAS/MACRO
  • SAS/GRAPH
  • CDISC SDTM
  • ADaM standards
  • analytical research databases
  • statistics
  • clinical trial concepts
  • data management concepts
  • drug/vaccine development

Nice to have

  • SAS programming
  • clinical trial programming
  • SAS/MACRO
  • SAS/GRAPH
  • SAS
  • R
  • Python
  • XML
  • Linked data
  • natural language processing
  • Unix/Linux environment
  • analysis plans
  • statistical terminology
  • statistical methods
  • statistical concepts
  • cross cultures and geographies
  • professional societies

What the JD emphasized

  • SAS programming experience in a clinical trial environment
  • Knowledge and understanding of CDISC SDTM and ADaM standards