Vibeke Miller Breinholt

Vice President
Nonclinical Development
Ascendis Pharma
Denmark

Business Expert Toxicology
Biography

educated toxicologist with more than 7 years of experience within the area of cancer and experimental cancer research and 12+ years within nonclinical safety in the biopharmaceutical industry. Proven leadership abilities of research projects and multifunctional teams within both discovery and development. Broad experience in designing and directing nonclinical development programs for biopharmaceuticals for various indications for both the European and the U.S. market; including management of the preclinical regulatory component of and strategy for regulatory submissions. Major strengths include a high level of innovation and productivity, a quality-oriented and strategic mindset and a strong competency within the areas of toxicology/nonclinical safety and nonclinical regulatory affairs.  

Research Intrest

Leadership/management, toxicology, nonclinical safety, nonclinical regulatory affairs, biopharmaceuticals