Senior Advisor, Nonclinical Toxicology

Job Summary

Managing day-to-day operations for toxicology and safety pharmacology studies remotely, the full-time Senior Advisor, Nonclinical Toxicology will oversee data flow between external CROs and internal teams, coordinate study protocols, and ensure compliance with regulatory requirements.

Key responsibilities

• Manage end-to-end data flow between external CROs and internal teams to ensure alignment with study objectives
• Initiate and execute draft SOWs with CROs in collaboration with project representatives
• Monitor nonclinical studies at CROs to ensure scientific quality and compliance with global regulations

Required qualifications

• BSc or MSc in toxicology, pharmacology, or a related discipline
• Minimum 6 years of experience in biotechnology or pharmaceutical industry focusing on nonclinical toxicology/safety pharmacology
• Strong understanding of biological sciences and nonclinical research methodologies
• Proficient in scientific data analysis software and data management systems
• Highly organized with proven ability to manage multiple studies and timelines