Research Scientist - Safety Assessment Toxicology

Job Overview

As an experienced Research Scientist for our Safety Assessment Toxicology team located in Laval, you will be overseeing study conduct of preclinical efficacy and/or toxicology studies. Multidisciplined expertise and oversight of client projects with varied dose routes, durations and complexities, the role expands to include scientific leadership in standard and non-standard preclinical models, technical oversight of studies, project management, and client interaction/collaboration. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Design and oversee with prospective and current clients program strategies and support commercial groups in the preparation of statement of work;
• Function as an independent Study Director in accordance with the applicable Good Laboratory Practice regulations (GLPs);
• Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities;
• Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments;
• Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances;
• Writes, reviews, and edits, as necessary, draft or final reports that document all study related procedures and results;
• Prompt verbal or written communication with Sponsors on study related business;
• Oversees and coordinates study conduct (Study Plan development, technical guidance, and reporting);
• Works on programs of moderate to difficult complexity;
• Involvement in design, development and/or performance of new procedures;
• May prepare abstracts for scientific publication;
• Presents collaborative or independent research internally or externally;
• Provides technical and scientific guidance to research staff;
• Functions as departmental representative for interdepartmental communications and initiatives as required.

Key Elements

We are looking for the following minimum qualifications for this role:

• Doctorate in health-related disciplines;
• At least 5 years of relevant experience in a preclinical environment as a scientist/researcher;
• Good interpersonal and communication skills;
• Strong problem-solving skills;
• Strong organizational skills.

Role Specific Information:

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Daytime Monday to Friday;
• Hybrid position - Half on-site & half remote (subject to change depending on the business needs);
• Permanent position as of the hiring, full-time 37.5hrs per week.
• Salary: The hiring range for this position is $73,000 to $99,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications and location.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.