Job Description
ABOUT THE COMPANY
Own the statistical strategy behind our clinical evidence — designing efficient studies, extracting publishable insights, and translating data into decisions that convince clinicians and regulators (FDA/CE).
ABOUT THE ROLE
Support ongoing clinical trials and regulatory interactions (FDA/Notified Bodies).
RESPONSIBILITIES
- Mass validation planning and analysis for pre‑clinical and multi‑center campaigns
- Design new clinical studies: protocols, SAPs, CRFs, endpoint definitions
- Optimize trial efficiency: reduce patient burden while preserving statistical significance
- Create publishable outputs: figures, tables, narratives for manuscripts and posters
- Contribute to cross‑functional teams (R&D, QA/RA, Medical, Product)
QUALIFICATIONS
- MSc/PhD in Biostatistics, Statistics, Data Science, or Epidemiology
- 3+ years applying statistics to clinical, biomedical,...