State Licensed Principal Scientist

Job Summary

As a full-time State Licensed Principal Scientist, the successful candidate will oversee non-clinical research activities for multiple projects in Translational Medicine/Preclinical Safety, ensuring compliance with study protocols and regulatory guidelines while working remotely.

Key responsibilities

• Formulates and leads novel projects, collaborating with teams to meet technical and scientific requirements
• Acts as the primary scientific contact for Study Directors at Contract Research Organizations (CROs) and oversees study progress
• Ensures compliance with GLP regulations and internal policies, resolving study-related issues and tracking timelines

Required qualifications

• PhD or MVSc/MS/M.Pharm with 7+ years of experience in drug discovery and/or development
• In-depth knowledge of toxicology assays in early development and safety pharmacology
• Proficient in techniques and processes used in drug design and development
• Strong logistical and planning abilities, with excellent communication skills
• Registration and certification with an International Toxicology organization