I’m Dr. Nadine Häusler, a consultant specialising in patient-centred evidence strategies for biotech, medtech, and CRO partners.

With over ten years of experience in epidemiology, biostatistics, and real-world evidence, I help teams design and implement Clinical Outcomes Assessment (COA) and patient-centred evidence strategies that align with regulatory and payer expectations. My work has contributed to successful FDA and EMA submissions, optimised clinical trial designs, and strengthened product value communication.

Before starting my independent practice, I worked at IQVIA, supporting global clients in integrating patient experience data into clinical development. Earlier in my career, I led academic research in epidemiology and biostatistics at the University Hospital Lausanne and University of Zurich, publishing several peer-reviewed studies.

I’m passionate about translating complex data into clear, actionable insights — helping companies bring meaningful, patient-focused innovation to market with scientific rigour and purpose.