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Added 12 mins ago
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Charles River Laboratories

Research Scientist II - Toxcology

Montreal, QC, Canada

Salary: The hiring range for this position is $73,000 to $99,000. · Full-time

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Job details

Pay: Salary: The hiring range for this position is $73,000 to $99,000.
Job type: Full-time
Apply by: Nov 27, 2026
Experience: Minimum of 5 years’ related experience in the research industry.
Posting language: English
Posted: Oct 28, 2026

Original job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

Research Scientist II - Toxicology

As a Research Scientist II for our Toxicology team at the Senneville location, you will be responsible for planning, coordinating, and overseeing study activities to ensure compliance with regulatory standards and high-quality scientific outcomes.

In This Role, Primary Responsibilities Include

Execute and manage studies of moderate to high complexity;
Design, write, review, and edit study plans, amendments, and study schedules to effectively define and organize all study-related activities;
Oversee and coordinate all aspects of study procedures, whether conducted within the department or in collaboration with external service groups;
Monitor project scope, staffing, and equipment needs; communicate effectively with leadership on resource planning;
Support proposal development and project management under supervision;
Participate in the design, development, and implementation of new procedures;
Prepare scientific abstracts and present research findings internally and externally as appropriate;
Act as a departmental representative in cross-functional initiatives and communications;
Prepare, review, and finalize draft and final reports documenting all study procedures, data, and results in a clear and accurate manner;
Host client visits, lead or support facility tours, and participate in client meetings (telephone/video conferences);
Mentor junior staff and support training of research scientists;
Ensure all projects are executed in accordance with Standard Operating Procedures (SOPs) and Good Laboratory Practice (GLP) regulations, while maintaining up-to-date knowledge of relevant regulatory guidelines.

Key Elements

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

Minimum of a bachelor’s degree (BA/BSc) in toxicology, pharmacology, or a related discipline.
Minimum of 5 years’ related experience in the research industry.
Proven ability to oversee and coordinate study conduct, including protocol development, technical guidance, and reporting
Strong understanding of the full study lifecycle, from proposal development through to final report completion
Demonstrated experience designing and reviewing study plans, amendments, and study schedules
Experience writing, reviewing, and editing draft and final reports that accurately document study procedures and results
Excellent attention to detail with strong scientific writing and organizational skills.
Excellent project management and organizational abilities
In-depth knowledge of GLP and regulatory requirements
Ability to coordinate cross-functional teams and manage multiple priorities

Role Specific Information

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1 ;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station, John Abbott College and from the REM station of l’Anse à l’Orme to the Senneville site. Free parking. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Monday-Friday, Day schedule with 6 weekends per year;
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. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications and location

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

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.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

236941

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More about this job

Responsibilities

Plan, coordinate, and oversee toxicology studies of moderate to high complexity, ensuring compliance with SOPs, GLP, and applicable regulatory requirements. Develop and review study plans and reports, manage resources and cross-functional activities, communicate findings, support clients, and mentor junior staff.

Requirements

Requires a bachelor’s degree in toxicology, pharmacology, or a related discipline and at least five years of related research-industry experience. Candidates should have strong study lifecycle, protocol and report writing, GLP and regulatory knowledge, project management, organizational, and cross-functional coordination skills.

Skills

Toxicology
Study Management
Study Protocol Development
Scientific Writing
Report Writing And Review
Good Laboratory Practice
Regulatory Compliance
Project Management
Cross-Functional Coordination
Resource Planning
Study Scheduling
Procedure Development
Data Documentation
Client Communication
Staff Mentoring
Training

Benefits

Performance Bonus
Free Shuttle Service
Free Parking
Electric Vehicle Charging Station
Free On-Site Gym
Employee And Family Assistance Program
Career Development Opportunities
Telemedicine
Four Weeks Of Vacation
Ten Personal Days
Social Activities
Health And Wellness Coverage
Stock Purchase Program
Work-Life Balance Flexibility

Visa sponsorship

Not detected in the job text

Keywords

Toxicology
Pharmacology
Safety Assessment
Preclinical Drug Development
Good Laboratory Practice
Standard Operating Procedures
Regulatory Guidelines
Regulatory Compliance
Study Lifecycle
Study Plans
Study Amendments
Study Schedules
Study Protocols
Scientific Reports
Scientific Abstracts
Project Management
Proposal Development
Cross-Functional Teams
Resource Planning
Staffing
Equipment Planning
Procedure Development
Data Documentation
Client Meetings
Research Industry

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