About me
Dr. Ulrike Kochendoerfer has over 20 years of experience in pharmaceutical research. She started her career in pre-clinical research in toxicology and biochemistry, before entering the regulatory medical writing field in 2005. Dr. Kochendoerfer holds a PhD from the University of Bonn/Germany in Genetics. Dr. Kochendoerfer managed medical writing teams in global submissions across multiple therapeutics areas and has extensive experience in Medical Writing Operations as well as Clinical Trial Disclosure. She is a member of DIA and AMWA.
