Senior Manager, Statistical Programming

Ipsen

Lead programmer managing multi-study statistical programming for a biopharmaceutical company. Ensuring quality and timely delivery of programming outputs for regulatory submissions and health authority responses.

Posted 7/10/2026full-timeParis • 🇫🇷 FranceSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in SAS programming and statistical analysis within the pharmaceutical and biotech sectors, ensuring high-quality deliverables and compliance with industry standards. Proficient in CDISC guidelines and experienced in clinical trial data management and reporting.

Highest-signal resume keywords

SAS ProgrammingCDISC StandardsSDTM ProgrammingADaM ProgrammingClinical Trials Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical ProgrammingData AnalysisTFL ProgrammingProgramming Standards DevelopmentQuality Assurance

Soft Skills

LeadershipCollaborationCommunication

Industry Keywords

PharmaceuticalBiotechCRODrug DevelopmentClinical Data Management

About the role

Key responsibilities & impact

Perform as a lead programmer on multiple compounds/studies within the Statistical Programming function
Ensure the quality and timeliness of all the deliveries (in house or outsourced)
Contribute to ensuring the oversight of all outsourced programming work to quality, budget, and timeline
Ensure the quality of Statistical Programming deliverables, including tables, listings, figures, datasets, and associated documentation
Participate in the development and implementation of SAS programming standards, SOPs, and work instructions
Ensure study-related documentation according to Ipsen processes and in a ready state acceptable for audit

Requirements

What you’ll need

Proficiency in statistical programming package(s), SAS is required
Familiar with Global Clinical Data Interchange Standards Consortium (CDISC)
Experience in SDTM and ADaM specification and programming
Experience in reporting and TFL programming
8+ years’ programming experience in pharmaceutical/biotech/CRO environment in drug discovery/clinical trials/drug development
Bachelor's or MSc in Statistics, Mathematics, or Scientific Discipline
Must be fluent in English
French is preferred

Benefits

Comp & perks

Collaborates and communicates without boundaries
Coaches and ensures decisions are made by consent
Plans and aligns effectively
Looks for opportunities to continually improve ways of working
Fosters a culture of collaboration, excellence and impact