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Pharmacovigilance Associate Jobs in Quebec (NOW HIRING)

CA$75K/yr

Job Overview As an Associate for our Pharmacokinetics team at the Senneville location, you will be responsible for the entire pharmacokinetic (PK) analysis process, including the communication of ...

$47/hr

Our associates deliver a higher standard of business services to support medical care and ... Maintain and demonstrate working knowledge of pharmacology, including drug reaction/overdose

$60/hr

Our associates deliver a higher standard of business services to support medical care and ... Maintain and demonstrate working knowledge of pharmacology, including drug reaction/overdose

$60/hr

Our associates deliver a higher standard of business services to support medical care and ... Maintain and demonstrate working knowledge of pharmacology, including drug reaction/overdose

$47/hr

Our associates deliver a higher standard of business services to support medical care and ... Maintain and demonstrate working knowledge of pharmacology, including drug reaction/overdose

$45/hr

Our associates deliver a higher standard of business services to support medical care and ... Maintain and demonstrate working knowledge of pharmacology, including drug reaction/overdose

Pharmacovigilance Associate information

See Quebec salary details

$24

$38

$51

How much do pharmacovigilance associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for pharmacovigilance associate in Quebec is $38.17, according to ZipRecruiter salary data. Most workers in this role earn between $30.05 and $44.95 per hour, depending on experience, location, and employer.

What is a pharmacovigilance associate?

A Pharmacovigilance Associate is responsible for monitoring, collecting, assessing, and reporting adverse drug reactions (ADRs) to ensure patient safety. They work with regulatory authorities, healthcare professionals, and pharmaceutical companies to analyze drug safety data. Their duties include case processing, literature screening, signal detection, and ensuring compliance with pharmacovigilance regulations. This role is vital for minimizing drug-related risks and maintaining regulatory compliance.

What are the typical daily responsibilities of a pharmacovigilance associate?

A Pharmacovigilance Associate is responsible for collecting, reviewing, and processing reports of adverse drug reactions, ensuring that all data is accurate and submitted in accordance with regulatory timelines. On a daily basis, you may enter case information into specialized safety databases, conduct follow-ups with healthcare professionals or patients for additional details, and assist in preparing safety reports for regulatory authorities. The role often involves close collaboration with medical, regulatory, and quality assurance teams to support comprehensive drug safety monitoring. You may also participate in ongoing training or audits to maintain compliance with evolving industry standards.

What are the key skills and qualifications needed to thrive as a pharmacovigilance associate?

To thrive as a Pharmacovigilance Associate, you need a strong background in life sciences or pharmacy, attention to detail, and a solid understanding of drug safety regulations. Familiarity with safety databases such as Argus or ARISg, as well as knowledge of global regulatory guidelines like FDA and EMA requirements, is often required. Strong analytical thinking, effective communication, and organizational skills help you manage case reports and collaborate with cross-functional teams. These skills are essential for accurately assessing and reporting adverse drug reactions to ensure patient safety and regulatory compliance.

Is pharmacovigilance a good career path?

Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, with roles like Pharmacovigilance Associate focusing on adverse event reporting and data analysis. It offers opportunities for career advancement, requires attention to detail, and often involves working with regulatory guidelines and safety databases. Many professionals find it a stable and rewarding career in the healthcare and pharmaceutical industries.

What qualifications do I need for pharmacovigilance?

A pharmacovigilance associate typically needs a bachelor's degree in pharmacy, medicine, life sciences, or a related field. Relevant skills include knowledge of drug safety regulations, data analysis, and experience with safety databases or case management tools; certifications such as the Drug Safety Certification (DSC) can also be beneficial.

What are the most commonly searched types of Pharmacovigilance jobs in Quebec?

The most popular types of Pharmacovigilance jobs in Quebec are:

What are popular job titles related to Pharmacovigilance Associate jobs in Quebec?

For Pharmacovigilance Associate jobs in Quebec, the most frequently searched job titles are:

What job categories do people searching Pharmacovigilance Associate jobs in Quebec look for?

The top searched job categories for Pharmacovigilance Associate jobs in Quebec are:

What cities in Quebec are hiring for Pharmacovigilance Associate jobs?

Cities in Quebec with the most Pharmacovigilance Associate job openings:

Infographic showing various Pharmacovigilance Associate job openings in Quebec as of August 2026, with employment types broken down into 1% As Needed, 55% Full Time, 32% Part Time, 1% Temporary, and 11% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $79,386 per year, or $38.2 per hour.

CA$75K/yr

Full-time

Medical, Retirement, PTO

Re-posted 29 days ago


Charles River Laboratories rating

8.4

Company rating: 8.4 out of 10

Based on 94 frontline employees who took The Breakroom Quiz

23rd 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 for our Pharmacokinetics team at the Senneville location, you will be responsible for the entire pharmacokinetic (PK) analysis process, including the communication of results within the context of preclinical studies.

In this role, primary responsibilities include:

  • Gather and consolidate relevant information related to pharmacokinetics (PK) and toxicokinetics (TK) studies;
  • Review and draft study plans/protocols for PK and TK studies, including amendments and preparation of PK/TK phase plans;
  • Perform data tabulation, conduct preliminary analyses, and generate summary results while demonstrating a strong understanding of PK processes and timelines;
  • Conduct pharmacokinetic analyses (non-compartmental analysis), interpret results, and prepare associated scientific reports;
  • Independently use PK platform tools, including Phoenix, PK Assist, and Integral.
  • Communicate proactively and effectively with the Study Director (SD), clients, and involved scientists (IS and/or PI);
  • Independently identify, analyze, and resolve issues related to production activities and scientific methodologies, in collaboration with the PK team;
  • Perform quality control (QC) review of PK/TK data, analysis and reports to ensure accuracy and compliance;
  • Maintain active scientific awareness in pharmacokinetics, including literature review and integration of relevant advancements, as well as proficiency with analysis software (e.g., WinNonlin and other PK parameter estimation tools).

 

Key Elements

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

  • Baccalaureate in science or other advanced degrees preferred;
  • A minimum of 2 years’ experience as PK associate;
  • Proficient in performing non-compartmental analysis (NCA) using the PK modeling and analysis platforms; Phoenix WinNonlin and PK Assist (mandatory);
  • Experienced with ‘Integral’ for data integration, study management, and PK/TK data review;
  • Proficiency in French and English, both spoken and written.

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 and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
  • Salary: $75,000 annually;
  • Schedule: Monday-Friday with possible weekends when needed;
  • 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 & 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.

 

Contact information: annabelle.landry@crl.com / (438) 469 – 8575

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.


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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