Principal Statistical Programmer (clinical Trials)

IQVIA

Mexico City, Mexico
Sas programming proficiency
Cdisc standards (adam, sdtm)
Develop and validate datasets
The Principal Stat Programmer ensures accuracy and integrity of statistical programming in clinical projects, demanding SAS proficiency and CDISC standards

Job Summary

  • The Principal Stat Programmer ensures accuracy and integrity of statistical programming in clinical projects, demanding SAS proficiency and CDISC standards.
  • Key responsibilities include developing and validating complex datasets, collaborating with cross-functional teams, and providing technical guidance.
  • The role involves mentoring junior programmers, contributing to workflow improvements, and leading initiatives to enhance programming tools and techniques.

Matching Summary

The Principal Stat Programmer ensures accuracy and integrity of statistical programming in clinical projects, demanding SAS proficiency and CDISC standards.

Skills & Requirements

Must-have

  • SAS programming proficiency
  • CDISC standards (ADaM, SDTM)
  • Develop and validate datasets
  • Clinical trial projects
  • Advanced English communication

Nice-to-have

  • Immunology therapeutic area experience
  • Neuroscience therapeutic area experience
  • Lead and manage programming teams
  • Inspire and motivate teams

Key Requirements

  • 2+ years efficacy analysis (ADaM datasets & TLF’s)
  • 4+ years ADAM statistical programming
  • Bachelor's Degree Statistics or Computer Science
  • Proficiency in R programming language
  • Ability to lead/manage others
  • Maintain confidential information
  • Sound judgment and decision-making
  • Effective time and resource management
  • Strong project management skills
  • Robust technical aptitude
  • Analyze and interpret financial data
  • Effective problem-solving skills
  • Strong written and verbal communication skills

Work Rights

Not specified

Tailored Resume

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