You act as Team Leader Rodent Toxicology with 5 direct scientific reports and direct a reproductive toxicology laboratory.
As Study Director in nonclinical in vivo safety studies (non GLP and GLP) you focus on developmental and reproductive toxicology (DART) studies as well as rodent toxicology studies.
You provide nonclinical safety expertise in drug development teams and participate in compilation of regulatory documents (e. g. IB, IND, DSUR) and safety assessments.
A special area of your toxicological expertise will be DART and the regulatory guidance connected to this field, where you support development teams on DART topics.
You contribute to developing our laboratory in vivo methods in the spirit of the 3R