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Added 3 hours ago
PC
Salesforce Platform Owner
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Competitive Benefits. Meaningful Extras. Unmatched Value.
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Clinical Trial Financial Control Analyst, Oncology Portfolio
RI-MUHC | Research Institute of the MUHC | #rimuhc
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- Full-time
We are seeking a Clinical Trial Financial Control Analyst to provide independent financial control and reconciliation for Oncology-sponsored clinical research studies. Reporting within the…
Added 3 hours ago
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Accounts Receivable Analyst
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management analyst
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Senior Business Analyst, Change Management
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- Full-time
…clearly define business needs, objectives, scope, expected benefits, resource requirements, risks, and dependencies. Ensure required analysis and deliverables are complete, accurate, and…
Added 19 hours ago
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Junior Tax Analyst
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Transformation Senior Analyst
Aston Carter
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- $100 to $110 CAD / hour
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The Middle & Back Office Change Management Transformation Senior Analyst supports a major transformation initiative by translating future-state Operations, Performance, Accounting, and…
Added 21 hours ago
MH
Behaviour Interventionist - Abbotsford
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- $21 to $23 CAD / hour
- Part-time
…team (of speech pathologists, by a Board-Certified Behavior Analyst® BCBAs, Occupational therapists and physical therapists) to clients receiving services from Monarch House. You will work…
Added 22 hours ago
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Trading Support Analyst
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Added 22 hours ago
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Senior Analyst Custody Invoicing
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Added 22 hours ago
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Collections Analyst - Bilingual (French)
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Toronto, ON · Hamilton, ON · Mississauga, ON · Cambridge, ON · Milton, ON · Canada Corporate (KC)
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…solving problems? Join Uline as a Bilingual (French) Collections Analyst, where you’ll help manage customer accounts, support timely payments and work with teams to ensure legendary service…
Added 23 hours ago
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IMAX is seeking a Business Analyst to bridge business functions, technology teams, data teams, project management, and senior leadership in defining and delivering technology-enabled…
Added 23 hours ago
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…Delivery and Procurement) is seeking a PeopleSoft Senior Systems Analyst to support the Workforce Information Network (WIN) system - a business-critical Oracle PeopleSoft HCM 9.2…
Added 1 day ago
CR
Scientist I
Charles River Laboratories
Montreal, QC
- Full-time
At least 18 months’ experience in an Analyst position or equivalent;
Added 1 day ago
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Bilingual (French and English) Service Support Analyst
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Charles River Laboratories

Scientist I

Montreal, QC, Canada

Salary: The hiring range for this position is between $61,000 to $78,000 per year. · Full-time

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Job details

Pay: Salary: The hiring range for this position is between $61,000 to $78,000 per year.
Job type: Full-time
Apply by: Nov 23, 2026
Posting language: English
Posted: Oct 24, 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

As a Scientist for our Immunogenicity team at the Senneville location, you will collaborate with the Analysts and other technical staff in scientific matters associated with the conduct, interpretation and reporting of studies.

In This Role, Primary Responsibilities Include

Involved in writing and/or reviewing study schedules, study plans, amendments and analytical procedures;
Communicate with Study Directors and Sponsors on study related business. Generate and distribute Client Interaction Reports (CIRs) in a timely manner;
Oversee and coordinate all aspects of study related Laboratory Procedures;
Review and approve raw data;
Notify the Lab Science management of technical problems or deviations from budgeted costs as soon as they become apparent.

Key Elements

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

Minimum of a Bachelor in Immunology, Biology or related discipline;
Hands-on experience in Ligand Binding assays or cell-based assays (eg. Immunogenicity);
At least 18 months’ experience in an Analyst position or equivalent;
Experience working in a Good Laboratory Practices (GLP) environment;
Ability to work under time constraints and adapt to change;
Good time management & problem-solving skills;
Strong interpersonal and communication skills;
Ability to lead work in a team environment.

Role Specific Information

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. In addition, the site is accessible from the Anse-à-l’Orme REM station via STM bus services. Free parking. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime schedule;
Permanent position as of the hiring, full-time 37.5hrs per week;
Salary: The hiring range for this position is between $61,000 to $78,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, 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);
3 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.

235919

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More about this job

Responsibilities

Collaborate with analysts and technical staff to conduct, interpret, and report immunogenicity studies, including preparing or reviewing study schedules, plans, amendments, and analytical procedures. Coordinate laboratory procedures, communicate with study directors and sponsors, prepare client interaction reports, review raw data, and promptly escalate technical issues or budget deviations.

Requirements

A bachelor's degree in immunology, biology, or a related discipline is required, along with hands-on experience in ligand binding or cell-based assays and at least 18 months of analyst-level or equivalent experience. Candidates must have GLP experience and demonstrate adaptability, time management, problem-solving, strong communication, and the ability to lead work in a team environment.

Skills

Immunology
Ligand Binding Assays
Cell-Based Assays
Immunogenicity
Good Laboratory Practices
Study Plan Writing and Review
Analytical Procedures
Raw Data Review
Client Communication
Study Reporting
Time Management
Problem-Solving
Interpersonal Communication
Team Leadership
Adaptability

Benefits

Performance-Based Annual Bonus
Free On-Site Gym
Employee and Family Assistance Program
Career Development Opportunities
Telemedicine and Access to Health Professionals
Three Weeks of Vacation
Ten Personal Days
Social Activities
Free Parking
Electric Vehicle Charging Station
Shuttle Service

Visa sponsorship

Not detected in the job text

Keywords

Immunogenicity
Immunology
Biology
Ligand Binding Assays
Cell-Based Assays
Good Laboratory Practices
GLP
Study Schedules
Study Plans
Study Amendments
Analytical Procedures
Laboratory Procedures
Raw Data
Client Interaction Reports
Study Directors
Sponsors
Study Conduct
Study Interpretation
Study Reporting
Technical Deviations
Budget Monitoring
Preclinical Drug Development
Safety Assessment
Contract Research Organization
Biotechnology Research

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