Lead Statistical Programmer-SAS/R & Regulatory Submissions

IQVIA Inc; Paris; On-site; EUR 90,000 - 130,000; Full time

Job summary

IQVIA is seeking an experienced Principal Statistical Programmer to provide technical leadership across Phase I-IV clinical trials in Paris. You will drive the delivery of high-quality statistical programming solutions and support regulatory submissions.

You will lead programming activities, mentor teams, and collaborate with Biostatistics, Data Management and Clinical groups to implement reusable tools and ensure compliance with CDISC standards.

Qualifications

• Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related field.
• Minimum 8+ years of statistical programming experience within pharma/biotech/CRO.
• 2+ years as Study Lead/Lead Programmer or equivalent across trials.

Responsibilities

• Lead statistical programming activities across multiple clinical studies.
• Serve as Study Lead with oversight and mentorship to programming teams.
• Develop, validate, and review TLFs using SAS and R.
• Drive standards, efficiencies, and process improvements.
• Prepare programming specifications and validation plans for submissions.
• Ensure high-quality regulatory submission packages.
• Collaborate with cross-functional teams to resolve data issues.
• Develop reusable programming tools and solutions.

Skills

SAS Base/Macro

R programming

CDISC SDTM/ADaM

Study Lead

Regulatory submissions

Statistical programming

Leadership

Education

Bachelor's/Master's in statistics or related field

Tools

SAS

R

Pinnacle 21

Job description

IQVIA is seeking an experienced Principal Statistical Programmer to provide technical leadership across Phase I-IV clinical trials in Paris. You will drive the delivery of high-quality statistical programming solutions and support regulatory submissions.

You will lead programming activities, mentor teams, and collaborate with Biostatistics, Data Management and Clinical groups to implement reusable tools and ensure compliance with CDISC standards.