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

IQVIA

Lima Metropolitana

Remote

PEN 310,000 - 448,000

Full time

14 days+

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Job summary

IQVIA Argentina is seeking a Principal Stat Programmer to ensure integrity of statistical programming across clinical projects. Proficiency in R and SAS is essential, with CDISC ADaM/SDTM familiarity. You will lead, mentor, and collaborate to improve workflows and deliver high-quality outputs.

Strong English skills are required; LATAM native language (Spanish/Portuguese) is preferred. This is a 100% home-based role with sponsor support, emphasizing innovation and methodological rigor.

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 on clinical trials.
  • Hands-on proficiency in R programming (mandatory).
  • Proficiency in SAS programming language.
  • Advanced English (written and spoken).
  • Native LATAM language required: Spanish or Portuguese.

Responsibilities

  • Develops and validates complex datasets and outputs using SAS, adhering to CDISC ADaM/SDTM standards.
  • Collaborates with cross-functional teams to optimize statistical programming processes.
  • Provides technical guidance on statistical methodologies and programming best practices.
  • Mentors junior programmers and supports their development.
  • Drives continuous improvement of programming workflows and departmental standards.
  • Delivers high-quality outputs by following established protocols and best practices.
  • Leads initiatives to enhance programming tools and techniques for innovation.
  • Aligns programming objectives with organizational goals with leadership coordination.

Skills

Leadership
Mentoring
Project management
Communication skills
Problem solving
Time management
Team collaboration
Advanced English

Education

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

Tools

SAS
R
CDISC ADaM/SDTM

Job description

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 https://jobs.iqvia.com

IQVIA 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.

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