Lead Statistician Clinical Trials - Cdi- M/f

Pierre Fabre

Toulouse, France
Statistical analysis of clinical trials
Sas or r programming
Clinical trial design
The Biometry Department supports all drugs being developed by Pierre Fabre, encompassing Data Management, Programming, and Statistics for clinical trials and Real-World evidence studies

Job Summary

  • The Biometry Department supports all drugs being developed by Pierre Fabre, encompassing Data Management, Programming, and Statistics for clinical trials and Real-World evidence studies.
  • Key responsibilities include participating in trial design, providing statistical guidance, drafting study documents, programming analyses, interpreting results, and preparing regulatory submissions.
  • Pierre Fabre offers an attractive remuneration/benefits package including incentives, profit-sharing, shareholding, health insurance, and additional holidays.

Matching Summary

The Biometry Department supports all drugs being developed by Pierre Fabre, encompassing Data Management, Programming, and Statistics for clinical trials and Real-World evidence studies.

Skills & Requirements

Must-have

  • Statistical analysis of clinical trials
  • SAS or R programming
  • Clinical trial design
  • Oncology clinical trials
  • Regulatory guidelines (ICH, EMA, FDA)

Nice-to-have

  • Agile and adaptable
  • Collaborative spirit
  • Rigorous and pragmatic approach
  • Creativity and proactivity
  • Real world evidence studies

Key Requirements

  • 6+ years experience in pharmaceutical industry or CRO
  • Advanced degree in Statistics or related field
  • Experience in clinical trial development
  • Strong experience in oncology clinical trials

Work Rights

Not specified

Tailored Resume

Cover Letter