MSc in Medical Biotechnology from the Technical University of Berlin, and a PhD in Molecular Biology from the University of Oslo.

Julia acts as a liaison between the trial site, medical authorities and other relevant third parties. Her responsibilities include the planning and overseeing of clinical trials, determining whether a product has achieved the goal for which it was produced, ensuring that products meet all government regulations and standards, and managing external stakeholders.

Julia has more than 8 years of experience in pharmaceutical and health sector related companies. She is a specialist in study startup activities such as feasibility, site selection, contract negotiations, IEC applications, ICF adaptations, all aspects of site management, and all other study related aspects.