Full-time jobs in Canada (341,421 jobs)

Explore full-time jobs across Canada. Choose a location and read the full job details.

341,421 listings · 49,598 employers Counted Nov 14, 2026. How we count

About these jobs

Employers hiring include Walmart Canada (7,196 listings), A&W Canada (4,234 listings), Loblaw Companies Limited (2,848 listings).

Common roles: Cook, Store manager, Sales representative.

89,545 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / hour	25.00	55,055
CAD / year	80,000.00	31,892
CAD / month	4,875.50	730
USD / year	134,450.00	410
CAD / day	223.15	132
CAD / week	1,600.00	97
USD / hour	20.00	37
GBP / year	270,000.00	24
EUR / year	65,000.00	11
GBP / hour	35.00	10

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 1% remote, 14% hybrid, 82% on-site, 2% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Full-time jobs in Canada

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Brunel

Pharmacovigilance Coordinator

ON, Canada

Full-time

Apply on brunel.net About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Feb 8, 2027
Experience: Experience: 3+ years of experience in pharmacovigilance, patient/drug safety.
Posting language: English
Posted: Nov 10, 2026

Original job description

Pharmacovigilance Coordinator (Contract ending October 2027) Remote - Ontario OR Quebec

Responsibilities

Adverse Event Management: Monitor, document, and report adverse events in compliance with regulatory guidelines.
Data Management: Enter and maintain accurate data in pharmacovigilance systems, ensuring timely updates and reports.
Communication: Serve as a liaison with internal and external stakeholders to address safety-related inquiries and provide updates.
Compliance: Ensure adherence to all relevant regulations, guidelines, and standard operating procedures.
Cross-Functional Collaboration: Work closely with cross-functional teams, including regulatory, quality assurance, and medical affairs, to align on safety processes and requirements.

Requirements

Bachelor's Degree in Science, or related field
Experience: 3+ years of experience in pharmacovigilance, patient/drug safety.
Language: French/English bilingual preferred.
Communication Skills: Strong verbal and written communication skills, with the ability to collaborate effectively across teams.
Attention to Detail: Exceptional ability to review and process detailed medical and regulatory forms accurately.
Independence: Self-starter with the ability to work independently and manage competing priorities.
Tech Savvy: Comfortable using pharmacovigilance systems, data management tools, and standard office software.
Adaptability: Ability to hit the ground running and adapt to evolving workflows and timelines.

What We OfferWhy apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We'll get you going while you get on with the job.

About Us

Brunel has a reputation for working with some of the best in the business. That's what we continually strive for. Over 45 years, we've created a global network of interesting clients and talented individuals working together through a vast array of services.

Apply on brunel.net About employer

More about this job

Responsibilities

The Pharmacovigilance Coordinator at Brunel will monitor, document and report adverse events under regulatory guidelines. They will keep pharmacovigilance data accurate and current, and work with regulatory, quality and medical affairs teams on safety processes.

Requirements

Brunel needs candidates with a science bachelor's degree and 3+ years of pharmacovigilance or patient or drug safety experience. Strong written and verbal communication, careful review of medical forms, independent work and comfort with safety and office software are required; French/English bilingualism is preferred.

Skills

Adverse event monitoring and reporting
Pharmacovigilance systems
Data management
Regulatory compliance
Standard operating procedures
Cross-functional collaboration
Stakeholder communication
Detail-oriented form review
Independent work
Office software
Bilingual French and English

Keywords

pharmacovigilance
drug safety
patient safety
adverse event reporting
adverse events
safety database
case processing
regulatory compliance
standard operating procedures
medical affairs
quality assurance
contract
remote
Ontario
Quebec
bilingual French English
clinical safety
pharmacy

Seniority

Mid level

Tools

pharmacovigilance systems
data management tools
standard office software

Languages

English
French

Fields of study

Science

Report this job

Work requirements

Full-time jobs in Canada