Senior Statistical Programmer in Pharmacometrics (PM) Support (Clinical Trials)

Location: 100% home-based from Mexico City, Mexico

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Develop and validate complex clinical-trial datasets and outputs using SAS.
• Apply CDISC standards, including ADaM and SDTM, to statistical programming deliverables.
• Provide technical guidance on statistical methodologies and programming best practices.
• Collaborate with cross-functional teams to improve programming processes, tools, and standards.
• Lead and mentor junior programmers while supporting programming teams and departmental objectives.
• Ensure accurate, high-quality deliverables within project timelines.

Requirements

• Bachelor’s degree in Statistics, Computer Science, or a related field.
• At least 2 years of experience with efficacy analysis, ADaM datasets, and TLFs, or at least 4 years of ADaM statistical programming experience in clinical trials.
• Hands-on proficiency in R and proficiency in SAS.
• Strong understanding of CDISC standards, statistical programming methods, and clinical-trial deliverables.
• Advanced English, written and spoken, with assessment during the interview process.
• Native Spanish or Portuguese is required for LATAM candidates.

Culture & Benefits

• 100% home-based sponsor-dedicated role.
• Opportunity to contribute to clinical research and healthcare projects.
• Work includes cross-functional collaboration, technical leadership, and continuous process improvement.
• Confidential handling of sensitive project data and internal communications is expected.