Principal Statistical Programmer (Clinical Trials)

IQVIA · Mexico City, Mexico

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Role summary

Principal Statistical Programmer responsible for developing and validating complex clinical trial datasets using SAS programming while ensuring CDISC standards compliance. The role involves mentoring junior programmers, collaborating across teams, and driving continuous improvement of statistical programming workflows and quality standards.

What they're looking for

Bachelor's degree in Statistics, Computer Science, or related field
2+ years efficacy analysis (ADaM datasets & TLFs) or 4+ years ADaM statistical programming in clinical trials
Proficiency in SAS programming language
Proficiency in R programming language
Advanced English language proficiency
Demonstrated ability to lead and manage programming teams
Experience in Immunology or Neuroscience therapeutic areas (highly valued)

What you'll be doing

Develop and validate complex datasets and outputs using SAS, ensuring CDISC ADaM and SDTM compliance
Mentor and guide junior programmers on technical methodologies and best practices
Collaborate with cross-functional teams to optimize statistical programming processes and accuracy
Lead initiatives to enhance programming tools, techniques, and departmental workflow standards
Deliver high-quality statistical programming outputs within established timelines and protocols

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Date posted16 days ago

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