Senior Statistical Programmer Lead - SAS & CDISC Expert

IQVIA; Barcelona; Presencial; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Principal Statistical Programmer to provide advanced technical expertise across complex studies, planning integrated programming solutions, and delivering statistical tables, figures and lists.

You will act as technical team lead, coordinate requirements with statisticians and clinical teams, mentor SP staff, and ensure adherence to CDISC/ADaM/SDTM standards while managing scope and timelines.

Formación

• Bachelor's degree in maths, computer science, statistics or related field.
• 7+ years’ statistical programming experience in life sciences.
• Strong efficacy experience.
• Advanced knowledge of statistics, programming and drug development processes.
• Advanced knowledge of Base SAS, SAS Graph and SAS Macro; CDISC/ADaM/SDTM.

Responsabilidades

• Plan, coordinate, and implement programming for complex studies (tables, figures, lists).
• Program analysis datasets and transfer files for internal/external clients.
• Perform programming QC checks and report data issues.
• Develop programming specifications from project requirements.
• Provide advanced technical expertise and deliver project solutions.
• Lead technical aspects for single/multiple complex studies and mentor SP staff.
• Communicate with internal and client statisticians to align timelines and requirements.
• Estimate scope, manage resources, and negotiate timelines for deliverables.
• Promote standards, SOPs, and best practices in programming.
• Provide training and mentoring to SP team members.

Conocimientos

Statistical programming

SAS programming

Project leadership

Stakeholder communication

CDISC/ADaM/SDTM

Clinical drug development

Data analysis datasets

Educación

Bachelor's degree in Maths/CS/Statistics

Herramientas

Base SAS

SAS Graph

SAS Macro

Descripción del empleo

IQVIA is seeking a Principal Statistical Programmer to provide advanced technical expertise across complex studies, planning integrated programming solutions, and delivering statistical tables, figures and lists.

You will act as technical team lead, coordinate requirements with statisticians and clinical teams, mentor SP staff, and ensure adherence to CDISC/ADaM/SDTM standards while managing scope and timelines.