Define appropriate strategies for Toxicology and Non-Clinical Pharmacology in assigned projects
Overall accountability for Toxicology and Non-Clinical Pharmacology strategies and activities in
Provide expert knowledge in Toxicology and Non-Clinical Pharmacology to the cross-functional teams
Responsible for Toxicology and Non-Clinical pharmacology modules and sections in regulatory
Responsible for interactions with regulatory authorities for all questions related to non-clinical
Manage preclinical safety studies in Contract Research Organizations: design, monitor, discuss and

🎯 Requirements

PhD, DVM or equivalent in relevant discipline with a minimum of five year experience as a project
Experience with biologics and small molecules is required, while experience with oligonucleotides
Board certification such as a DABT/ERT is a plus

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