Lead preclinical toxicology studies in Laval with Charles River as an experienced Research Scientist overseeing complex programs and client projects.

This Research Scientist supports the Safety Assessment Toxicology team through scientific leadership, study oversight, and project management. You will guide preclinical efficacy and toxicology studies across varied dose routes, durations, and complexities. The work includes technical oversight, regulatory compliance, reporting, and client collaboration.

Key Responsibilities:

- Design program strategies with prospective and current clients
- Function independently as a Good Laboratory Practice Study Director
- Develop Study Plans, amendments, and study schedules




- Coordinate procedures across departments and service groups
- Provide scientific guidance and communicate with Sponsors

Requirements:

- Doctorate in a health science related discipline
- Three to five years of relevant preclinical scientist experience
- At least one year of relevant industry experience
- Positive interpersonal and communication skills
- Strong problem solving and organizational skills

Apply scientific leadership, Good Laboratory Practice oversight, and toxicology expertise to preclinical research at Charles River.

📌 Safety Assessment Toxicology Scientist (Laval)
🏢 Charles River Laboratories
📍 Laval