Bridging Discovery and Development

My career in translational research spans over 15 years at renowned research institutions in the US like St. Jude Children's Research Hospital and the University of Tennessee Health Science Center, as well as the Research Center for Emerging Infections and Zoonoses in Germany.

Leading international research teams to develop antivirals and improved vaccines, I implemented hypothesis-driven approaches and rigorous pre-clinical experimental designs; both of which are critical for successful drug development.

My board-certification as a medical affairs specialist (BCMAS) ensures a strong foundation in knowledge and skills critical to various areas of medical affairs including clinical trials, pharmacovigilance, RWE and HOER, compliance, medical/scientific communication, regulatory affairs and MSL skills.

Today, I help biotech founders, pharma medical affairs teams, CROs and academic investigators apply this rigour to their most critical challenges. From designing preclinical experiments and clinical studies that generate regulatory-grade data to crafting funding proposals, I provide the strategic scientific expertise needed to move programs forward and accelerate research to meet milestones and timelines.

Core Expertise

Tailored support in writing, science, and medical affairs.

Let's Discuss Your Scientific Challenge