Category
General Administrative
Description
Tasks and responsibilities
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- You act as Team Leader Rodent Toxicology with 5 direct scientific reports and direct a reproductive toxicology laboratory.
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- 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.
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- You provide nonclinical safety expertise in drug development teams and participate in compilation of regulatory documents (e. g. IB, IND, DSUR) and safety assessments.
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- 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.
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- You contribute to developing our laboratory in vivo methods in the spirit of the 3R