Group Director - Safety Analytics And Reporting

Roche

Basel, Switzerland
Hybrid
Safety data science expertise
Pharmacoepidemiology
Complex safety information reporting
The Group Director of Safety Analytics and Reporting provides strategic leadership, expertise and oversight for safety data science, pharmacoepidemiology, analytical excellence and complex safety information reporting throughout the Roche product lifecycle

Job Summary

  • The Group Director of Safety Analytics and Reporting provides strategic leadership, expertise and oversight for safety data science, pharmacoepidemiology, analytical excellence and complex safety information reporting throughout the Roche product lifecycle.
  • This role integrates GxP safety knowledge with advanced safety data science expertise to support process experts across GVP, GCP, and medical devices safety.
  • The Group Director leverages the strengths of a diverse global team and creates an inspiring environment where the SAR team members feel empowered to take ownership of deliverables, build knowledge and deploy resources effectively, always striving for continuous improvement.

Matching Summary

The Group Director of Safety Analytics and Reporting provides strategic leadership, expertise and oversight for safety data science, pharmacoepidemiology, analytical excellence and complex safety information reporting throughout the Roche product lifecycle.

Skills & Requirements

Must-have

  • Safety data science expertise
  • Pharmacoepidemiology
  • Complex safety information reporting
  • GxP compliance
  • Real World Data/Evidence (RWD/E) strategy
  • AI/LLM understanding

Nice-to-have

  • Inspiring leadership environment
  • Continuous improvement focus
  • Cross-functional collaboration
  • Scientific rigour and creativity
  • Inclusive teamwork

Key Requirements

  • 10+ years PV/safety, clinical data, or pharmacoepidemiological analysis
  • 5+ years people leadership experience
  • 5+ years drug safety databases experience
  • Advanced degree in Data Science, Quantitative/Natural Sciences, or qualified health professional
  • Expert-level drug development lifecycle knowledge
  • Hands-on statistical analysis and medical data reporting mastery
  • Fluent in English

Work Rights

Not specified

Tailored Resume

Cover Letter