Nathalie Uzcat

Nathalie is an independent clinical and medical affairs consultant with a background spanning early-phase protocol design through to post-approval lifecycle support. She works closely with biotech and pharma teams to shape studies that are scientifically sound and operationally realistic, drawing on both clinical training and hands-on programme experience.

Nathalie partners with sponsors to identify where a study or programme most needs support — whether that's KOL engagement, medical writing, regulatory-facing documentation, or ongoing medical affairs oversight — and adapts her involvement accordingly. Her approach centres on clear communication between clinical, scientific, and regulatory stakeholders so that decisions stay grounded in the evidence.

She has worked across a range of settings including contract research, academic and clinical research units, and industry-facing medical affairs roles, giving her a practical view of how programmes move from early design through to real-world evidence generation. She holds a medical degree along with postgraduate qualifications in clinical and regulatory medicine, with research training grounded in Nordic and EU practice.