Senior Statistical Programmer - ADaM, SAS & R Lead

IQVIA Argentina; Warszawa; On-site; PLN 180,000 - 260,000; Full time

Job summary

IQVIA is seeking a Senior Statistical Programmer to design, develop and QC SAS programs for ADaM datasets, tables, figures and submission packages. This role collaborates with study teams to ensure submission readiness and adherence to CDISC standards.

You will lead programming activities for pooled and exploratory analyses, develop global tools to improve efficiency, and support regulatory responses and publications.

Qualifications

• BSc in Computer Science, Mathematics, Statistics or related area.
• At least 5+ years of experience in clinical or statistical programming.
• Extensive experience with SAS and SAS Macros; strong problem-solving skills.
• Good experience in R programming is mandatory.
• Advanced knowledge of CDISC standards (CDASH, SDTM, ADaM).
• Experience leading programming activities for pooled analyses across multiple studies.
• Ability to work independently or in a team and meet timelines.
• Experience in cross-functional, multicultural and international teams.

Responsibilities

• Review datasets in ADaM format and generate tables, figures and listings for submissions.
• Design, develop and QC SAS programs to access, transform and analyze clinical data.
• Collaborate with study teams to ensure submission readiness and data quality.
• Lead programming activities for pooled and exploratory analyses and deliver ISS/ISE datasets when needed.

Skills

SAS programming

R programming

CDISC standards

Analytical thinking

Education

BSc in Computer Science, Mathematics, Statistics or related area

Job description

IQVIA is seeking a Senior Statistical Programmer to design, develop and QC SAS programs for ADaM datasets, tables, figures and submission packages. This role collaborates with study teams to ensure submission readiness and adherence to CDISC standards.

You will lead programming activities for pooled and exploratory analyses, develop global tools to improve efficiency, and support regulatory responses and publications.