Senior Product Support Engineer — Linux & Security

Third-Party Job Posts; Quilmes; Remote; ARS 139,086,000 - 200,903,000; Full time

Job summary

IQVIA is seeking a Senior Statistical Programmer in Pharmacometrics for a 100% home-based role. The candidate will develop and validate datasets using SAS, ensure CDISC ADaM/SDTM compliance, and mentor junior programmers across clinical trials. Strong R skills and advanced English required.

The role requires leading cross-functional teams, guiding methodologies, and improving programming workflows to deliver high-quality results within deadlines.

Qualifications

• Bachelor's Degree in Statistics, Computer Science or related field.
• 2+ years with efficacy analysis (ADaM datasets & TLFs) and/or 4+ years on ADaM statistical programming in clinical trials.
• Hands-on proficiency in R programming language (mandatory).
• Proficiency in SAS programming language.
• Advanced English (both written and spoken).
• Native language is required - LATAM: Spanish or Portuguese.
• Ability to lead/manage others in programming teams.
• Demonstrated ability to maintain confidential information and meet deadlines.

Responsibilities

• Develops and validates complex datasets and outputs using SAS, ensuring CDISC ADaM/SDTM compliance.
• Collaborates with cross-functional teams to optimize statistical programming processes and efficiency.
• Provides technical guidance on statistical methodologies and programming best practices.
• Mentors junior programmers and contributes to process improvements.
• Ensures high-quality deliverables by adhering to standards 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

Advanced English

Leadership

Education

Bachelor's Degree in Statistics/Computer Science or related field

Job description

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

Mexico City, Mexico
Santiago, Chile
Buenos Aires, Argentina
Lima, Peru
Quito, Ecuador
São Paulo, Brazil
Bogota, Colombia
Full time
R
Sponsor dedicated - 100% Home based role.
Job Overview
The Principal Stat Programmer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in R and SAS programming and familiarity with CDISC standards, particularly ADaM and SDTM models. Key responsibilities include developing and validating complex data sets and outputs, collaborating with cross‑functional teams to optimize processes, and providing technical guidance on statistical methodologies and programming best practices. The role also involves mentoring junior programmers and contributing to the continuous improvement of programming workflows and standards, supporting the overall quality deliverables of the statistical programming department.
Essential Functions

• Develops and validates complex datasets and outputs using SAS programming, ensuring compliance with CDISC standards such as ADaM and SDTM models.
• Collaborates with cross‑functional teams to optimize statistical programming processes and enhance overall efficiency and accuracy.
• Provides technical guidance and expertise on statistical methodologies to support clinical trial projects and departments.
• Mentors and guides junior programmers, fostering their growth and development.
• Contributes to the continuous improvement of programming workflows and departmental standards.
• Ensures high‑quality deliverables from the statistical programming department by adhering to best practices and established protocols.
• Leads initiatives to enhance programming tools and techniques, driving innovation in statistical programming.
• Partners with leadership to align programming objectives with larger organizational goals.

Qualifications

• Bachelor's Degree Statistics, Computer Science or related field.
• 2 + years working with efficacy analysis (Adam datasets & TLF's) and/or 4 + years on ADAM statistical programming on clinical trials.
• Hands‑on proficiency in R programming language (mandatory).
• Proficiency in SAS programming language.
• Advanced English (both written and spoken - tested during the interview process).
• Native language is required - LATAM: Spanish or Portuguese.
• Ability to lead/manage others. Capably leads and manages programming teams, ensuring adherence to standards and mentoring junior programmers.
• Demonstrated ability to maintain confidential information, sensitive project data and internal communications.
• Exercises sound judgment and decision‑making in selecting statistical methods and programming techniques.
• Effectively manages time and resources to deliver high‑quality programming outputs within tight deadlines.
• Executes projects efficiently, demonstrating strong project management skills to coordinate tasks and resources effectively.
• Demonstrates robust technical aptitude with a deep understanding of SAS programming and CDISC standards.
• Analyses and interprets financial data accurately to make informed decisions in statistical programming.
• Applies effective problem‑solving skills to overcome programming challenges and optimize workflows.
• Exhibits strong written and verbal communication skills to document programming methodologies and procedures clearly to facilitate collaboration and improve statistical programming processes with cross‑functional teams.
• Inspires and motivates programming teams to align their work with organizational goals and quality standards.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled