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 ...
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 ...
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 ...
Montreal, QC · On-site
The Associate Director partners closely with sponsors and cross-functional teams to translate ... Collaborate with Nonclinical, Clinical, Toxicology, Pharmacology, DMPK, and Medical Writing teams ...
Montreal, QC · On-site
The Associate Director partners closely with sponsors and cross-functional teams to translate ... Collaborate with Nonclinical, Clinical, Toxicology, Pharmacology, DMPK, and Medical Writing teams ...
The Associate Director partners closely with sponsors and cross-functional teams to translate ... Collaborate with Nonclinical, Clinical, Toxicology, Pharmacology, DMPK, and Medical Writing teams ...
The Associate Director partners closely with sponsors and cross-functional teams to translate ... Collaborate with Nonclinical, Clinical, Toxicology, Pharmacology, DMPK, and Medical Writing teams ...
As an Associate Director (AD) Pharmacometrician , you'll lead high-impact modeling and simulation efforts within a dynamic Clinical Pharmacology, Modeling and Simulation (CPMS) environment. You'll ...
As an Associate Director (AD) Pharmacometrician , you'll lead high-impact modeling and simulation efforts within a dynamic Clinical Pharmacology, Modeling and Simulation (CPMS) environment. You'll ...
Veiller a ce que le personnel respecte les directives de pharmacovigilance et les exigences en ... Associate Program Manager is responsible for undertaking the management, planning, and ...
Veiller a ce que le personnel respecte les directives de pharmacovigilance et les exigences en ... Associate Program Manager is responsible for undertaking the management, planning, and ...
Montreal, QC · On-site
... pharmacovigilance) de Sante Canada, en fonction de son role attribue au moment de l'embauche et ... JOB SUMMARY Under the supervision of the Associate Program Manager, the Reimbursement Specialist ...
Montreal, QC · On-site
... pharmacovigilance) de Sante Canada, en fonction de son role attribue au moment de l'embauche et ... JOB SUMMARY Under the supervision of the Associate Program Manager, the Reimbursement Specialist ...
$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
$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
$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
$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
$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
Montreal, QC · On-site
... and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP ... For Real World Late Phase, the CRA II will use the business card title of Site Management Associate ...
Montreal, QC · On-site
... and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP ... For Real World Late Phase, the CRA II will use the business card title of Site Management Associate ...
... and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP ... For Real World Late Phase, the CRA II will use the business card title of Site Management Associate ...
... and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP ... For Real World Late Phase, the CRA II will use the business card title of Site Management Associate ...
$24.52 - $26.94
4% of jobs
$26.94 - $29.37
17% of jobs
$30.38 is the 25th percentile. Wages below this are outliers.
$29.37 - $31.80
9% of jobs
$31.80 - $34.22
4% of jobs
The median wage is $36.29 / hr.
$34.22 - $36.65
18% of jobs
$36.65 - $39.07
18% of jobs
$40.36 is the 75th percentile. Wages above this are outliers.
$39.07 - $41.50
8% of jobs
$41.50 - $43.92
4% of jobs
$43.92 - $46.35
4% of jobs
$46.35 - $48.78
4% of jobs
$48.78 - $51.20
8% of jobs
$24
$38
$51
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.
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.
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.
The most popular types of Pharmacovigilance jobs in Quebec are:
For Pharmacovigilance Associate jobs in Quebec, the most frequently searched job titles are:
The top searched job categories for Pharmacovigilance Associate jobs in Quebec are:
Cities in Quebec with the most Pharmacovigilance Associate job openings:

CA$75K/yr
Full-time
Medical, Retirement, PTO
Re-posted 29 days ago
8.4
Based on 94 frontline employees who took The Breakroom Quiz
23rd of 86 rated pharmaceutical
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.
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:
We are looking for the following minimum qualifications for this role:
Role Specific Information:
Why Charles River ?
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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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.
Scientific research and development services
10,000+ Employees
Wilmington, MA, US
1947