Lead Statistician – Real World Evidence -cdi- M/f

Pierre Fabre

Toulouse, France
Incentives; profit-sharing; shareholding with matc...
Hybrid (2 days per week from home)
Advanced degree in statistics or related field
Minimum 6 years pharmaceutical industry experience
Significant involvement in real world evidence studies
Pierre Fabre is seeking a Lead Statistician with expertise in Real World Evidence (RWE) studies to join their Biometry Department in Toulouse or Boulogne, France. The role requires advanced statistical skills, proficiency in SAS, and a collaborative spirit to contribute to both RWE and randomized controlled trials

Job Summary

  • The role involves participating in the conception and design of Real-World Evidence studies while providing expert statistical support.
  • Candidates will act as the primary point of contact for statistical aspects, contributing to regulatory submissions for agencies like the FDA and EMA.
  • The position offers an attractive remuneration package including incentives, profit-sharing, shareholding matching, and 41 days of holidays.

Matching Summary

Match Score: 85

Pierre Fabre is seeking a Lead Statistician with expertise in Real World Evidence (RWE) studies to join their Biometry Department in Toulouse or Boulogne, France. The role requires advanced statistical skills, proficiency in SAS, and a collaborative spirit to contribute to both RWE and randomized controlled trials.

Salary

Incentives; Profit-sharing; Shareholding with matching contribution

Skills & Requirements

Must-have

  • Advanced degree in Statistics or related field
  • Minimum 6 years pharmaceutical industry experience
  • Significant involvement in Real World Evidence studies
  • Proficiency in SAS software for statistical analysis
  • Strong understanding of RWE study design and methodology
  • Familiarity with regulatory guidelines ICH EMA FDA NICE ENcEPP

Nice-to-have

  • Experience with interventional studies
  • Knowledge of CDISC standards
  • Creativity and proactivity in a matrix environment
  • Ability to manage multiple studies simultaneously
  • Collaborative spirit across Data Management and Programming teams

Key Requirements

  • Master's Degree, ENSAI, ISUP, or PhD in Statistics
  • 6+ years experience in pharma or CRO sector
  • Mandatory expertise in Real World Evidence methodologies

Work Rights

Not specified

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