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,...