Head of Project Toxicology

Experteer Overview

As VP, Head of Project Toxicology, you will define and lead Evotec’s safety assessment strategy across the drug discovery and development portfolio, enabling science‑driven decisions from concept to regulatory submission. You will be the key interface between discovery and development safety, shaping program direction, partnerships, and cross‑functional collaboration. You’ll lead a high‑performing toxicology team and work with senior leaders and global partners to deliver forward‑looking safety strategies. This role offers global, flexible work options and a meaningful impact on patient safety and program success.

Retribuzione / Benefits

• Own and advance the safety strategy for internal programs and external partnerships to keep the toxicology framework innovative and data‑driven
• Inspire, mentor, and develop a team of expert toxicologists with strategic direction and learning culture
• Guide safety strategy from Target Safety Assessment to Development Candidate nomination for both small and large molecules
• Serve as SME to Discovery and Development teams for regulatory toxicology studies enabling Phase 1 and beyond
• Build and maintain collaborative relationships with global clients to align safety strategy and program progress
• Foster integration and transparent communication across internal functions for cohesive portfolio decision‑making
• Model and cultivate ownership, trust, accountability, and empowerment across the team and organization

Responsabilità

• Extensive senior‑level Toxicology experience in biotech, pharma, and/or CRO environments
• Proven leadership of interdisciplinary, cross‑functional teams in a matrix setting
• Excellent communication and synthesis of complex data for risk‑balanced recommendations
• Track record of advancing programs from preclinical discovery into clinical development across modalities
• Deep expertise in preclinical drug discovery models and strategic alignment with development objectives
• Strong stakeholder management and collaboration across discovery, clinical, regulatory, and operational functions
• Experience preparing/contributing to IND/CTA submissions for small molecules and biologics
• Comprehensive knowledge of global regulatory safety guidelines across modalities
• Strong organizational and time‑management skills in fast‑paced environments
• Creative, strategic problem‑solver with growth mindset and adaptability