Remote Senior Statistical Programmer - Pharmacometrics

Jobrad Holding; Santiago; Remote; CLP 86,957,000 - 125,604,000; Full time

Job summary

IQVIA is seeking a Senior Statistical Programmer in Pharmacometrics for a 100% home based role. This position supports clinical trials across LATAM and beyond, delivering SAS-based datasets and outputs in CDISC ADaM/SDTM formats.

The ideal candidate has 4+ years in clinical trial programming, strong R and SAS skills, and fluent English. LatAm Spanish/Portuguese speakers are preferred. Join a global team and drive innovative programming solutions from a remote setting.

Qualifications

• Bachelor's Degree in Statistics, Computer Science or related field.
• 2+ years working with efficacy analysis (Adam datasets & TLFs) and/or 4+ years on ADaM statistical programming on clinical trials.
• Hands-on proficiency in R programming language.
• Proficiency in SAS programming language.
• Advanced English (written and spoken).
• Native language LATAM: Spanish or Portuguese.

Responsibilities

• Develops and validates complex datasets and outputs using SAS programming, ensuring CDISC ADaM/SDTM compliance.
• Collaborates with cross-functional teams to optimize programming processes.
• Provides technical guidance on statistical methodologies for clinical trial projects.
• Mentors junior programmers and guides team growth.
• Contributes to improvements in programming workflows and departmental standards.
• Ensures high-quality deliverables by adhering to best practices and protocols.
• Leads initiatives to enhance programming tools and techniques.
• Partners with leadership to align programming objectives with organizational goals.

Skills

R programming

SAS programming

Leadership

CDISC standards

Education

Bachelor's Degree in Statistics/CS or related field

Tools

R

SAS

Job description

IQVIA is seeking a Senior Statistical Programmer in Pharmacometrics for a 100% home based role. This position supports clinical trials across LATAM and beyond, delivering SAS-based datasets and outputs in CDISC ADaM/SDTM formats.

The ideal candidate has 4+ years in clinical trial programming, strong R and SAS skills, and fluent English. LatAm Spanish/Portuguese speakers are preferred. Join a global team and drive innovative programming solutions from a remote setting.