Jobs in Canada

25+ jobs

Group jobs by employerEmail me new jobs Save this search

Added 1 hour ago
WS
Senior Millwright
Wolf Steel Ltd
Barrie, ON
- Full-time
Work closely with the operations, engineering, and quality assurance teams to ensure machinery is aligned with production goals
Added 1 hour ago
WS
Senior Millwright
Wolf Steel Ltd
Barrie, ON
- Full-time
Shift: Day Shift - 7:00am to 3:30pm
Added 2 hours ago
W
OMNI Customer Fulfillment Associate (PT)
Walmart
Medicine Hat, AB
- Part-time
Working as an OMNI Customer Fulfillment Associate at Walmart Canada is a great opportunity to build valuable skills in a fast‑paced retail environment. In this role, you pick, pack, and…
Added 5 hours ago
GC
Associate Producer - EA SPORTS FC™ Mobile, Business Operations
Game Companies
Vancouver, BC
- Full-time
…teams, and players. EA Mobile is dedicated to creating high-quality mobile games connected to some of the world's biggest gaming franchises, with the current FIFA Mobile leading the…
Added 6 hours ago
AG
Inventory - Field Data Collector
Acosta Group
AB · Edmonton, AB
- Part-time
The Data Collection Associate is responsible for collecting and transmitting data gathered from designated retail stores primarily using a handheld device.
Added 6 hours ago
J
Engineering Project Manager - Developer Services
Jobgether
Canada
- Full-time
Review project documentation for completeness, quality assurance, conformity, and contractual compliance.
Added 7 hours ago
W
Project Manager
Worley
Edmonton, AB
- Full-time
…delivery of complex project scope in accordance with safety, quality, schedule and budget…
Added 10 hours ago
WC
Day Remodel Associate
Walmart Canada
Huntsville, ON
- Contract
Follows guidelines for cold chain compliance to ensure quality assurance.
Added 10 hours ago
WC
(CAN) Day Remodel Associate
Walmart Canada
Calgary, AB
- Contract
Follows guidelines for cold chain compliance to ensure quality assurance.
Added 10 hours ago
SF
Digital Expansion Associate - Simplii Financial
Simplii Financial
Toronto, ON
- Full-time
You need to be legally eligible to work at the location(s) specified above and, where applicable, must have a valid work or study permit
Added 11 hours ago
AW
VP & Head of Environmental, Canada
Allied World Assurance Company
Toronto, ON
- Full-time
Our people are our most important asset, and we are very proud of the quality of our team members.
Added 12 hours ago
LL
Dock Lead Hand- 2nd Shift
LINEAGE LOGISTICS HOLDINGS, LLC
Calgary, AB
- Full-time
…to make certain company and customer standards of service, quality, safety, and productivity are…
Added 12 hours ago
TU
Senior Research Analyst, Pharmacoepidemiology
The University of British Columbia
Victoria, BC
- $8,087.08 to $12,117.08 CAD / month
- Full-time
…analyze administrative database; writes, executes, and assess quality of SAS code to support CNODES projects and MoH deliverables; documents quality assurance testing and coding methods;…
Added 12 hours ago
CG
Chef Manager
Compass Group Canada
Saint-Hyacinthe, QC · St-Hyacinthe, QC
- Full-time
Ensure the unit has strict compliance with the Compass Quality Assurance and Health and Safety Program, Occupational Health and Safety Act and WHMIS regulations.
Added 12 hours ago
US
Warehouse Associate II - MHE
UPS Supply Chain Solutions
Calgary, AB
- Full-time
A Warehouse Associate II impacts the organization by meeting specific operational key performance indicators. This experienced employee has a general knowledge of warehousing terminology…
Added 12 hours ago
PC
Resourcing and Deployment Senior Associate, Assurance (Bilingual FR/EN)
Pwc Canada
Montreal, QC
- Full-time
As a Resourcing and Deployment Senior Associate, unlock your potential and embrace the chance to drive meaningful outcomes that’ll elevate your career. Your role will include, but isn’t…
Added 12 hours ago
UO
Senior Research Analyst, Pharmacoepidemiology
University of British Columbia
Victoria, BC · BOFF | Therapeutics Initiative (THRPI)
- $8,087.08 to $12,117.08 CAD / month
- Full-time
…analyze administrative database; writes, executes, and assess quality of SAS code to support CNODES projects and MoH deliverables; documents quality assurance testing and coding methods;…
Added 13 hours ago
W
(CAN) Bakery Associate
Walmart
Wainwright, AB
- Part-time
Working as a Bakery Associate at Walmart Canada is a great way to develop your skills in the retail industry. A Bakery Associate provides exemplary customer service by adhering to the basic…
Added 13 hours ago
Estate and Trust Associate, ScotiaTrust - Montreal (12 months contract)
Scotiabank
Montreal, QC
Provides quality assurance support that helps ETCs ensure their new business is submitted in good order. This includes ensuring that all documentation (original Will, Powers of Attorney,…
Added 13 hours ago
P
Accounting and Transaction Advisory Senior Associate (Bilingual FR/EN)
PwC
Montreal, QC
- Full-time
As an Accounting and Transaction Advisory Senior Associate you’ll work as part of a team of problem solvers, helping to solve business issues, deliver high quality client service and…
Added 13 hours ago
OC
Educational Developer
Olds College of Agriculture & Technology
Olds, AB
- $30 to $40 CAD / hour
- Contract
The intention is that the Educational Developer will work from the Olds campus 3 days per week
Added 13 hours ago
W
(CAN) Pharmacy Intern
Walmart
Bracebridge, ON
- Full-time
…achieve positive health outcomes and/or to maintain or improve quality of life for the…
Added 13 hours ago
W
(CAN) OMNI Customer Fulfillment Associate
Walmart
Orangeville, ON
- Part-time
Working as an OMNI Customer Fulfillment Associate at Walmart Canada is a great opportunity to build valuable skills in a fast‑paced retail environment. In this role, you pick, pack, and…
Added 13 hours ago
W
(CAN) OMNI Customer Fulfillment Associate (3 month Contract)
Walmart
Hanover, ON
- Part-time
Working as an OMNI Customer Fulfillment Associate at Walmart Canada is a great opportunity to build valuable skills in a fast‑paced retail environment. In this role, you pick, pack, and…
Added 13 hours ago
I
Technical Analyst - Mississauga, ON
Intertek
Mississauga, ON
- Full-time
Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter…

Closed listing

ICON San Antonio

Clinical Research Associate

Montreal, QC, Canada

Full-time

This opening has closed.

The original listing is kept below for reference.

Find open jobs More jobs with this employer

About employer

Job details

Job type: Full-time
Closing date: Oct 31, 2026
Posting language: English · French
Posted: Sep 6, 2026

Similar jobs hiring now

Search current openings

Original job description

Archived listing. The details below describe a past opening.

English section of this bilingual listing.

Clinical Research Associate - Quebec

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. We are looking for a CRA in Quebec City to monitor CV and respiratory studies.

What You Will Do

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required Qualifications And Experience

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Willingness to travel as required (approximately 60%)

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

Read the full bilingual original

Clinical Research Associate - Quebec

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. We are looking for a CRA in Quebec City to monitor CV and respiratory studies.

What You Will Do

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required Qualifications And Experience

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Willingness to travel as required (approximately 60%)

Conseiller(ère) principal(e) en recherche clinique (Senior CRA) – Ville de Québec

En tant que Conseiller(ère) principal(e) en recherche clinique (Senior CRA) chez ICON Plc, vous superviserez et gérerez les activités liées aux essais cliniques afin de garantir leur réalisation conformément aux protocoles, aux exigences réglementaires et aux normes de l’industrie. Nous sommes à la recherche d’un(e) CRA basé(e) à Québec pour assurer le suivi d’études en cardiovasculaire et respiratoire.

Ce que vous ferez

Vous dirigerez des activités de surveillance d’essais cliniques exigeant une solide expertise technique, avec un accent particulier sur la qualité et l’amélioration continue.

Principales Responsabilités

Effectuer le suivi des sites d’essais cliniques afin de s’assurer du respect des protocoles d’étude, des exigences réglementaires et des normes de Bonnes Pratiques Cliniques (BPC/GCP).
Réaliser des visites de sites pour évaluer leur performance, résoudre les problématiques et fournir le soutien nécessaire à la réussite des essais.
Collaborer avec des équipes multidisciplinaires afin d’assurer une collecte de données et une production de rapports exactes et réalisées dans les délais.
Offrir de la formation et du soutien au personnel des sites ainsi qu’aux autres ARC/CRA afin de maintenir des normes élevées de conduite des essais cliniques.
Établir et entretenir des relations de travail efficaces avec le personnel des sites et les principales parties prenantes afin de favoriser le bon déroulement des études.

Votre profil

Vous possédez de solides bases en surveillance d’essais cliniques ainsi que l’expérience nécessaire pour travailler de façon autonome et encadrer les autres.

Qualifications Et Expérience Requises

Baccalauréat dans une discipline scientifique pertinente ou dans un domaine lié aux soins de santé.
Expérience significative à titre d’Associé(e) de recherche clinique (CRA), avec une excellente compréhension des processus des essais cliniques et des exigences réglementaires.
Capacité démontrée à gérer simultanément plusieurs sites et projets, avec de fortes compétences en organisation et en résolution de problèmes.
Expertise des pratiques de surveillance clinique, de l’intégrité des données et de la gestion des sites, ainsi qu’une maîtrise des logiciels et outils pertinents utilisés dans les essais cliniques.
Excellentes habiletés en communication, en relations interpersonnelles et en gestion des parties prenantes, avec la capacité d’influencer les intervenants et de promouvoir la conformité dans un environnement complexe.
Disponibilité à voyager selon les besoins du poste (environ 60 % du temps).

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

About employer

More about this job

Responsibilities

Monitor clinical trial sites and conduct site visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice standards. Coordinate with cross-functional teams, support site staff and other CRAs, resolve site issues, and promote accurate, timely trial data and continuous quality improvement.

Requirements

A bachelor's degree in a relevant scientific or healthcare-related field and extensive Clinical Research Associate experience are required. Candidates should be able to manage multiple sites and projects, demonstrate expertise in monitoring, data integrity, and site management, communicate effectively with stakeholders, and travel approximately 60% of the time.

Skills

Clinical Trial Monitoring
Good Clinical Practice
Regulatory Compliance
Site Management
Data Integrity
Clinical Trial Protocols
Site Visits
Issue Resolution
Data Collection and Reporting
Staff Training
Stakeholder Management
Project Management
Organization
Problem-Solving
Communication
Clinical Trial Software

Benefits

Annual Leave
Health Insurance
Retirement Planning
Employee Assistance Programme
Life Assurance
Childcare Vouchers
Bike Purchase Schemes
Discounted Gym Memberships
Subsidized Travel Passes
Health Assessments

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research Associate
Clinical Trials
Clinical Trial Monitoring
Good Clinical Practice
Regulatory Requirements
Study Protocols
Cardiovascular Studies
Respiratory Studies
Site Visits
Site Performance
Site Management
Data Integrity
Data Collection
Reporting
Cross-Functional Collaboration
Clinical Trial Software
Staff Training
Stakeholder Management
Quality Improvement
Compliance
Clinical Trial Processes
Travel

Report this job

Work requirements

Jobs in Canada