Senior Principal Scientist (Study Monitor) Preclinical Safety (London)

Senior Principal Scientist (Study Monitor) Preclinical Safety

Job ID REQ-10057306

Date: July 15, 2025

Summary

The Preclinical Safety (PCS) department within the Biomedical Research (BR) - Translational Medicine Unit provides non-clinical safety strategies for products in discovery, development, and market, globally, with state-of-the-art regulatory compliance.

As a Scientific Study Monitor, you will oversee non-clinical research activities for multiple projects across various disease areas, focusing on in-vivo toxicity and/or in-vitro screening toxicity studies conducted at our CRO partner sites, acting as the primary scientific contact for the Study Director.

About the Role

Major accountabilities:

• Lead and coordinate novel projects within the team or across functions, generating innovative ideas to meet technical requirements and project goals.
• Serve as the primary scientific contact for outsourced preclinical studies, ensuring studies are conducted according to protocols, GLP regulations, and international standards.
• Oversee study progress, resolve issues, and communicate effectively with internal experts and external partners to ensure timely delivery of reports.
• Maintain knowledge of relevant regulations (Swiss medic, OECD, FDA) to support GLP-compliant toxicology studies.

Role Requirements:

• PhD or MVSc/MS/M.Pharm with 7+ years of experience in drug discovery or development, preferably as Study Director or Study Monitor in early preclinical GLP studies.
• Deep understanding of toxicology assays, safety pharmacology, and genotoxicity.
• Proficiency with techniques used in toxicology and drug development tools and processes.
• Excellent communication skills, team-oriented, with strong planning abilities.
• Registration with an international toxicology register is preferred.

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