Principal Biostatistician

IQVIA

Mexico
Fully remote
Statistical analysis plans (saps)
Sas and/or r programming
Cdisc sdtm and adam standards
This advanced-level position requires strong expertise in biostatistics and programming, with a focus on clinical development in the pharmaceutical or biotech industry

Job Summary

  • This advanced-level position requires strong expertise in biostatistics and programming, with a focus on clinical development in the pharmaceutical or biotech industry.
  • Key Responsibilities include authoring, QC, and implementing Statistical Analysis Plans (SAPs) with minimal oversight, and developing and validating SAS and/or R programs for tables, listings, and figures (TLFs).
  • Ensure compliance with CDISC SDTM and ADaM standards and produce statistical study reports, communicating results to clinical and cross-functional teams.

Matching Summary

This advanced-level position requires strong expertise in biostatistics and programming, with a focus on clinical development in the pharmaceutical or biotech industry.

Skills & Requirements

Must-have

  • Statistical Analysis Plans (SAPs)
  • SAS and/or R programming
  • CDISC SDTM and ADaM standards
  • end-to-end statistical support
  • linear mixed models
  • multivariate analysis
  • design of experiments
  • Bayesian statistics
  • R Markdown and Quarto

Nice-to-have

  • CNS therapeutic area experience
  • adaptive designs
  • real-world evidence analyses
  • excellent communication skills

Key Requirements

  • PhD in Biostatistics or Statistics
  • Minimum 5 years of experience
  • Advanced English proficiency
  • CMC experience
  • Proficiency in R language

Work Rights

Not specified

Tailored Resume

Cover Letter