Karolina Janikowska is a Clinical Affairs Manager at Neurosoft Bioelectronics, with extensive experience in clinical and regulatory affairs, particularly in the medical device sector. Previous roles include Senior Associate-Clinical and Regulatory Affairs Consultant and Project Associate at Medidee, where responsibilities encompassed medical writing, strategic regulatory planning, and clinical investigation management. Karolina has also served as a Clinical Study Coordinator at CHUV, R&D Analytical Manager at Sensient Technologies, and a Post-doctoral fellow at the University of Geneva, contributing to a range of research projects. Educational qualifications include a DAS in Clinical Trial Management and a PhD in Organic Chemistry from Gdańsk University of Technology.