Head of Project Toxicology

Job not on LinkedIn

🔥 0 minutes ago

🌐 United Kingdom, Italy, +2 more countries – Remote

🇬🇧 United Kingdom – Remote 🇮🇹 Italy – Remote 🇫🇷 France – Remote 🇩🇪 Germany – Remote

⏰ Full Time

🔴 Lead

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Evotec

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1993

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

Healthcare • Manufacturing • Biotechnology

Evotec is a biotechnology company specializing in R&D and pipeline co-creation partnerships across various therapeutic and disease areas. The company leverages its AI-powered R&D platforms such as PanOmics and iPSC technologies to enhance disease understanding and human relevance. Evotec provides CRO/CDMO services, using cutting-edge continuous manufacturing technology and AI to improve access to high-quality biotherapeutics. Through its innovative business models, Evotec aims to deliver efficient and cost-effective solutions to unmet medical needs in collaboration with its partners.

📋 Description

• Define and lead the safety assessment strategy across Evotec’s drug discovery and development portfolio • Drive science-based safety decision-making from early concept through regulatory submission • Serve as the key interface between discovery and development safety • Shape program direction and strengthen strategic partnerships across modalities and therapeutic areas • Lead and develop a high-performing team of toxicology experts • Own and advance the safety strategy for internal programs and external partnerships • Guide safety strategy from Target Safety Assessment through Development Candidate nomination • Support design, execution, and interpretation of regulatory toxicology studies for Phase 1 clinical trials and beyond • Build collaborative relationships with global clients and align on safety strategy • Foster integration and cohesive decision-making across internal functions

🎯 Requirements

• Extensive senior-level experience in Toxicology within biotech, pharma, and/or CRO environments • Experience leading interdisciplinary, cross-functional teams in a complex matrix setting • Exceptional communication and scientific synthesis skills • Track record advancing programs from preclinical discovery into clinical development across multiple modalities and therapeutic areas • Deep expertise in preclinical drug discovery models • Experience managing stakeholder dynamics, resolving conflict, and collaborating across discovery, clinical, regulatory, and operational functions • Experience preparing and contributing to successful IND/CTA submissions for small-molecule and biologic programs • Comprehensive knowledge of global regulatory safety guidelines • Strong organisational and planning capabilities, attention to detail, and time-management skills • Creative, strategic problem-solving, adaptability, curiosity, and openness to new approaches and emerging science • BSc, MSc, or PhD in Toxicology, Pharmacology, Biology, or a related scientific discipline, with substantial relevant experience • DBAT, ERT, UKRT or equivalent professional certification is desirable

🏖️ Benefits

• Flexible working arrangements available • Equal employment opportunities and inclusive workplace • Safe, diverse, and inclusive workplace built on mutual respect