IQVIA

Principal Biostatistician

IQVIA

full-time

Posted on:

Location Type: Remote

Location: Argentina

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Job Level

About the role

  • Author, QC, and implement Statistical Analysis Plans (SAPs)
  • Develop and validate SAS and/or R programs for tables, listings, and figures (TLFs)
  • Perform QC/peer review and validation of statistical programs
  • Produce statistical study reports and communicate results to clinical and cross-functional teams
  • Review and contribute to statistical sections of study protocols

Requirements

  • Minimum 5 years of experience in biostatistics/statistics
  • Strong programming skills in SAS and/or R
  • Expertise in QC and validation processes
  • Solid understanding of clinical trial design and analysis methods
  • PhD in Biostatistics or Statistics (nice to have)
  • Experience in CNS therapeutic area (nice to have)
Benefits
  • Health insurance
  • Professional development
  • Paid time off
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
SASRStatistical Analysis PlansQCvalidation processesstatistical programmingclinical trial designdata analysis methods
Soft Skills
communicationcollaboration
Certifications
PhD in BiostatisticsPhD in Statistics