About Charles River Charles River is an early-stage contract research organization (CRO). We have ... Charles River also provides a suite of products and services to support our clients' clinical ...
New
About Charles River Charles River is an early-stage contract research organization (CRO). We have ... Charles River also provides a suite of products and services to support our clients' clinical ...
New
$230 - $370/hr
... clinical services for infants and children with extra-cranial solid tumor and related cancer ... The Department of Pediatrics is affiliated with CHEO, the CHEO Research Institute and the ...
$230 - $370/hr
... clinical services for infants and children with extra-cranial solid tumor and related cancer ... The Department of Pediatrics is affiliated with CHEO, the CHEO Research Institute and the ...
Company Description MEDFAR Clinical Solutions was founded in 2010 by two aeronautical engineers who ... Apply knowledge acquired as an Associate * Manage more complex email cases * Handle regular phone ...
Quick apply
Company Description MEDFAR Clinical Solutions was founded in 2010 by two aeronautical engineers who ... Apply knowledge acquired as an Associate * Manage more complex email cases * Handle regular phone ...
Clinical Research Associate Intern information
See Quebec salary details
$8.89 - $13.94
5% of jobs
$18.19 is the 25th percentile. Wages below this are outliers.
$13.94 - $18.99
23% of jobs
$18.99 - $24.04
19% of jobs
The median wage is $25.05 / hr.
$24.04 - $29.09
11% of jobs
$29.09 - $34.13
10% of jobs
$38.24 is the 75th percentile. Wages above this are outliers.
$34.13 - $39.18
9% of jobs
$39.18 - $44.23
7% of jobs
$44.23 - $49.28
5% of jobs
$49.28 - $54.33
5% of jobs
$54.33 - $59.37
3% of jobs
$59.38 - $64.42
2% of jobs
$8
$31
$64
How much do clinical research associate intern jobs pay per hour?
As of Sep 4, 2026, the average hourly pay for clinical research associate intern in Quebec is $31.55, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $40.62 per hour, depending on experience, location, and employer.
What does a clinical research associate intern do?
A Clinical Research Associate Intern assists in the monitoring and coordination of clinical trials to ensure they are conducted according to regulatory standards and study protocols. Interns may help with site visits, data collection, documentation, and communication between research teams and sponsors. This role provides hands-on experience in clinical research processes and helps interns develop an understanding of Good Clinical Practice (GCP) guidelines. Interns often work under the supervision of experienced clinical research professionals and gain valuable insight into the pharmaceutical or medical device industry.
What are the key skills and qualifications needed to thrive as a clinical research associate intern, and why are they important?
To thrive as a Clinical Research Associate Intern, you need a solid understanding of clinical trial protocols, regulatory guidelines (like GCP), and typically a background in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like GCP training are highly valued. Strong attention to detail, organizational skills, and effective communication help interns excel in monitoring studies and collaborating with site staff. These skills are crucial for ensuring data integrity, regulatory compliance, and the smooth operation of clinical research projects.
What typical challenges do clinical research associate interns encounter when monitoring clinical trial sites?
Clinical Research Associate Interns often face challenges such as ensuring accurate data collection, maintaining regulatory compliance, and communicating effectively with site staff. Balancing these responsibilities while learning industry protocols can be demanding, especially when managing multiple sites or studies. Interns are supported by experienced team members, but must quickly adapt to varying site workflows and documentation standards to ensure trial integrity.
What is the difference between Clinical Research Associate Intern vs Clinical Research Coordinator?
| Aspect | Clinical Research Associate Intern | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Typically pursuing or holding a degree in life sciences; some internships require minimal certifications | Usually holds a bachelor's degree in health sciences or related field; certifications like CCRP are common |
| Work Environment | Internship setting within pharmaceutical companies or research institutions; supervised learning | Active role in clinical trial sites; responsible for daily trial operations |
| Employer & Industry Usage | Used by pharmaceutical companies, CROs, and research institutions for training | Employed directly at clinical sites, hospitals, or research centers |
While both roles involve clinical trial processes, a Clinical Research Associate Intern is primarily a learning position focusing on gaining experience, whereas a Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites.
What are popular job titles related to Clinical Research Associate Intern jobs in Quebec?
For Clinical Research Associate Intern jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate Intern jobs in Quebec look for?
The top searched job categories for Clinical Research Associate Intern jobs in Quebec are:
What cities in Quebec are hiring for Clinical Research Associate Intern jobs?
Cities in Quebec with the most Clinical Research Associate Intern job openings:
Full-time
Medical, Retirement, PTO
Posted 3 days ago
New
Key responsibilities
Support Laboratory Scientists in preparing study deliverables such as assay results tabulation and study reports while ensuring compliance with GLP, SOP, AP, and study plans.
Prepare and review analytical procedures, forms, and study documentation to ensure study quality and facilitate submission for review and audit.
Collaborate with cross-functional teams to support study completion and contribute to the preparation of study plans, reports, and study summaries.
Charles River Laboratories rating
8.3
Based on 95 frontline employees who took The Breakroom Quiz
24th of 86 rated pharmaceutical
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 an Associate Scientist for our Immunology team at the Sherbrooke location, you will support supports the Laboratory Scientists in preparing study deliverables, such as assay results tabulation and study reports, while respecting timelines and preserving a quality of work compliant with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans.
In this role, primary responsibilities include:
- Prepare and review analytical procedures, forms, and related study documentation to ensure study quality and compliance.
- Coordinate the submission of documentation, data, and supporting materials for review and audit.
- Collaborate with cross-functional teams across Charles River Laboratories to support study completion.
- Perform and/or review the tabulation and analysis of study results.
- Contribute to the preparation of study plans and study reports.
- Prepare or review study summaries, including MQS and MVS documentation.
- Partner with Scientists to compile study deliverables and ensure they are audit-ready for Quality Assurance (QA) review.
- Address QA findings and support the resolution of audit observations.
Key Elements
We are looking for the following minimum qualifications for this role:
- Minimum of a College diploma in Sciences related discipline;
- Hands-on experience in ELISA, ligand-binding, immunogenicity (ADA), TK, and/or multiplex assay techniques.
- Work effectively within multidisciplinary teams to support study execution and deliverables.
- Demonstrate professionalism, strong communication skills, and positive working relationships.
- Adapt efficiently to changing priorities and tight timelines in a regulated laboratory environment.
- Contribute to departmental performance and quality improvement initiatives.
- Communicate effectively in both English and French.
Role Specific Information:
- Location: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5.
- Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
- Salary: As per internal equity and salary scale
- Annual bonus based on performance.
- Schedule: Regular working hours are daytime, Monday to Friday. Additional hours may be required periodically to meet business needs and project deadlines.
- Permanent, full-time position requiring a minimum of 37.5 hours per week, starting upon hire.
Why Charles River ?
- We offer competitive benefits and advantages from day one to support your well-being;
- Paid development training;
- 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 & 5 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.
What Charles River Laboratories employees say
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Benefits
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About Charles River
Sourced by ZipRecruiter
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 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 supported the development of 86% of the drugs approved by the FDA in 2021.
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Wilmington, MA, US
Year founded
1947