Senior Statistical Programmer & Project Lead

IQVIA; Paris; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

IQVIA in Paris seeks a Principal Statistical Programmer to lead complex programming activities across studies, develop process methodologies, and provide internal consulting on specifications and user needs.

You will plan and coordinate integrated programming solutions, mentor SP team members, and ensure adherence to CDISC/ADaM/SDTM standards while collaborating with statisticians and clinical teams.

Qualifications

• Bachelor's degree or higher in a relevant field.
• 7+ years of statistical programming experience in life sciences.
• Strong efficacy experience.
• Advanced knowledge of statistics, programming and clinical drug development.
• Advanced knowledge of Base SAS, SAS Graph and SAS Macro.
• Advanced knowledge of CDISC/ADaM/SDTM.

Responsabilités

• Plan, coordinate, and implement programming for complex studies, including creation of tables, figures, and lists.
• Program analysis datasets and transfer files for clients.
• Perform programming QC checks and address data issues.
• Develop programming specifications from project requirements.
• Provide advanced technical expertise and lead project solutions for SP teams.
• Mentor SP team members and train colleagues.
• Communicate with statisticians and clinical teams to align requirements and timelines.
• Estimate scope, allocate resources, and negotiate timelines.

Connaissances

Statistical programming

Efficacy experience

Clinical drug development

SAS programming

CDISC/ADaM/SDTM knowledge

Formation

Bachelor's degree in Maths, CS, Statistics or related field

Outils

Base SAS

SAS Graph

SAS Macro

Description du poste

IQVIA in Paris seeks a Principal Statistical Programmer to lead complex programming activities across studies, develop process methodologies, and provide internal consulting on specifications and user needs.

You will plan and coordinate integrated programming solutions, mentor SP team members, and ensure adherence to CDISC/ADaM/SDTM standards while collaborating with statisticians and clinical teams.