Use GLP expertise to coordinate regulated research studies for Charles River’s Inhalation team in Senneville, Quebec. The position is full-time.

This Research Scientist II position oversees study conduct from proposal development through final report completion. You will design study schedules, coordinate cross-functional activities, and maintain regulatory compliance. The role also includes project management, scientific documentation, and guidance for junior research staff.

Key Responsibilities:

- Oversee study procedures within departments and external groups
- Develop proposals and support project management under supervision
- Implement recent procedures and departmental initiatives
- Finalize reports documenting procedures, data, and results




- Mentor junior staff and support research scientist training

Requirements:

- Bachelor’s degree in toxicology, pharmacology, or related field
- At least five years of related research industry experience
- Demonstrated study planning and scheduling experience
- Excellent project management and organizational abilities
- Ability to manage multiple priorities across functional teams

Bring study lifecycle knowledge, project management, and regulatory understanding to Charles River’s Inhalation research team.

📌 GLP Study Coordination Scientist (Montreal)
🏢 Charles River Laboratories
📍 Montreal