Lead Statistician, Real-World Evidence (RWE) – Remote

Pierre Fabre Group; Toulouse; Hybride; EUR 90 000 - 120 000; Plein temps

Avantages offerts par ce poste

Incentives

Profit-sharing

Shareholding with matching

Health and provident insurance

RTT holidays and personal holidays

Public transport subsidy

Résumé du poste

Pierre Fabre Group is seeking a Lead Statistician – Real World Evidence to join the Biometry Department in Toulouse (Oncopôle) or Boulogne. The role is full-time, remote or hybrid, and involves leading RWE studies and contributing to clinical trials within a matrixed team.

Key duties include designing studies, developing SAPs, and guiding statistical analyses while coordinating with Data Management, Programming, and Medical Writing to support regulatory submissions.

Qualifications

• Advanced degree in statistics or related field with strong quantitative skills.
• Experience in pharmaceutical industry or CRO with Real-World Evidence studies.
• Proficiency in SAS and/ or other statistical software; ability to implement complex analyses.
• Familiarity with regulatory guidelines (ICH, EMA, FDA) and CDISC standards.
• Excellent written and verbal communication in English.

Responsabilités

• Design Real-World Evidence studies, determine sample size, objectives, and evaluation criteria; write SAPs.
• Act as statistical lead; attend meetings and provide guidance on analyses.
• Collaborate with vendors and CROs; evaluate proposals and manage deliverables.
• Draft and validate documents (protocols, CRFs, SAPs, study reports) with timely delivery.
• Program and validate analyses in SAS; communicate results to clinicians and regulatory teams.

Connaissances

Advanced statistics

SAS

Real-World Evidence

Clinical trials

Regulatory knowledge

English proficiency

Biostatistics

Formation

Master's degree in Statistics

Outils

SAS

CDISC

Description du poste

Pierre Fabre Group is seeking a Lead Statistician – Real World Evidence to join the Biometry Department in Toulouse (Oncopôle) or Boulogne. The role is full-time, remote or hybrid, and involves leading RWE studies and contributing to clinical trials within a matrixed team.

Key duties include designing studies, developing SAPs, and guiding statistical analyses while coordinating with Data Management, Programming, and Medical Writing to support regulatory submissions.