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).

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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...