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Data Reviewer Jobs in Quebec (NOW HIRING)

CA$114K - CA$127K/yr

... reviews, cybersecurity event response procedure) as applicable Create lightweight training and enablement (how-to guides, governance playbooks, onboarding for dashboard users and data owners)

CA$114K - CA$127K/yr

Support security and compliance needs (vendor assessments for data tools, audit readiness, risk reviews, cybersecurity event response procedure) as applicable * Create lightweight training and ...

Experience in data review a major asset; * Excellent command of English and French required, in accordance with industry requirements. The perfect candidate is passionate about the pharmaceutical ...

About The Role The QC reviewer, LBA is responsible to perform the quality control for data generated and work conducted in the laboratory. What You'll Do Here * Ensures that all batch related ...

Work with data engineers to specify data needs, review pipelines, and address data quality. * Develop and maintain performance indicators and metrics relating to production, cost, revenue, and ...

Work with data engineers to specify data needs, review pipelines, and address data quality. * Develop and maintain performance indicators and metrics relating to production, cost, revenue, and ...

... review without losing the thread. Primary Responsibilities * Set strategy. Own the multi-year data ... strategy supporting Operating Model optimization and TailorCare's extension beyond MSK; frame ...

Support audits, inspections, and management reviews with analytical insights * Contribute to ... Relevant experience in data analysis, preferably within HSE, industrial, or construction ...

Our Talent Acquisition team will review your profile to ensure it aligns with our requirements and ... Define a build data tracking methods and processes * Work with engineers to create data tracking ...

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Showing results 1-20

Data Reviewer information

See Quebec salary details

$13

$23

$39

How much do data reviewer jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for data reviewer in Quebec is $23.73, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $34.86 per hour, depending on experience, location, and employer.

What is the difference between Data Reviewer vs Data Analyst?

AspectData ReviewerData Analyst
Required CredentialsTypically a bachelor's degree in data management, IT, or related fields; certifications like CDMP are commonBachelor's degree in statistics, data science, or related fields; certifications like CAP or Microsoft certifications are common
Work EnvironmentMostly office-based, working with data validation tools and softwareOffice or remote, analyzing data sets, creating reports, and visualizations
Employer & Industry UsageUsed in industries like finance, healthcare, and government for data quality assuranceUsed across industries for data-driven decision making and reporting

While both roles involve working with data, Data Reviewers focus on validating and ensuring data accuracy, whereas Data Analysts interpret data to generate insights. Understanding these differences helps in choosing the right career path or job search focus.

What Is the Job of a Data Reviewer?

A data reviewer helps an organization review and interpret data for accuracy and interpretation. Data reviewers are necessary for many fields, including software development, quality assurance, medical and health care professions, and accounting, to name a few. Your responsibilities and duties are to look through collected data that has been entered into a spreadsheet or other database. You check it for any errors and manage issues you find. Some data reviewer positions, such as in medical research, include an analytical component; you help the research team to glean insight from the collected data.

What are Data Reviewers?

Data Reviewers are professionals responsible for examining, verifying, and validating data to ensure its accuracy, completeness, and compliance with established standards or regulations. They typically work with large datasets, reviewing and identifying errors or inconsistencies, and may also recommend or implement corrective actions. Data Reviewers play a crucial role in maintaining the quality and reliability of information used in various industries, such as healthcare, finance, and research.

What are the key skills and qualifications needed to thrive as a Data Reviewer, and why are they important?

To thrive as a Data Reviewer, you need strong analytical skills, attention to detail, and typically a background in life sciences, statistics, or a related field. Familiarity with data management systems, electronic data capture (EDC) platforms, and compliance standards such as GCP is commonly required. Excellent problem-solving, critical thinking, and communication skills help you identify discrepancies and collaborate with cross-functional teams. These competencies are crucial for ensuring data integrity, regulatory compliance, and the reliability of research outcomes.

How does a Data Reviewer typically collaborate with other teams to ensure data quality?

Data Reviewers work closely with data entry specialists, analysts, and project managers to verify the accuracy and consistency of datasets. They often participate in cross-functional meetings to discuss data discrepancies and establish best practices for data validation. This collaboration helps maintain high-quality data standards and ensures that any issues are promptly identified and resolved, supporting the overall goals of the organization.
What are popular job titles related to Data Reviewer jobs in Quebec? For Data Reviewer jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Data Reviewer jobs in Quebec look for? The top searched job categories for Data Reviewer jobs in Quebec are:
What are popular job titles related to Data Reviewer jobs in QC? For Data Reviewer jobs in QC, the most frequently searched job titles are:
Infographic showing various Data Reviewer job openings in Quebec as of June 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 44% In-person, 17% Hybrid, and 39% Remote job distribution, with an average salary of $49,350 per year, or $23.7 per hour.
Data Reviewer - Clinical Pathology

Full-time

Medical, Retirement, PTO

Posted 11 days ago


Charles River Laboratories rating

8.2

Company rating: 8.2 out of 10

Based on 91 frontline employees who took The Breakroom Quiz

25th of 71 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 a Data Reviewer for our Clinical Pathology team at the Laval location, you will verify data for completeness and Good Laboratory Practice (GLP) compliance, and you will promote awareness of best practices related to data collection.

In this role, primary responsibilities include:

  • Perform review of supporting data and complex clinical pathology data;
  • Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP) and the Institutional Animal Care and Use Committee (IACUC) rules.  

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

  • College diploma in science;
  • Minimum of 3 years’ experience working in a Good Laboratory Practices (GLP) environment;
  • Ability to work under time constraint and adapt to change;
  • Demonstrate flexibility and ability to work independently.

Role Specific Information:

 

  • Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
  • Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
  • Salary: $23/hrs;
  • Annual bonus based on performance;
  • Schedule: Monday to Friday, daytime schedule. Depending on the business needs, you may have to do overtime;
  • Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

  • We offer competitive benefits and advantages from day one to support your well-being;
  • 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

Pay

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Workplace

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Charles River logo

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