Find work in Canada.

320,719 jobs across our Canadian network. How we count

Jobs in Canada

25+ jobs

Email me new jobs Save this search

Added just now
RETAIL STORE COORDINATOR FULL TIME WINNERS
TJX Canada – Winners, Marshalls, HomeSense
Calgary, AB
Full-time
Support for you and your family through our Associate and Family Assistance programs, offering helpful resources and services to enhance your well-being.
Added just now
Store Coordinator
TJX Canada – Winners, Marshalls, HomeSense
Westbank, BC
Full-time
Support for you and your family through our Associate and Family Assistance programs, offering helpful resources and services to enhance your well-being.
Added just now
Office Associate
Bronte Electrical Corp.
Burlington, ON
Full-time
Role Description The Office Associate is a full-time, on-site role located in Burlington, ON, responsible for supporting daily office operations and providing administrative assistance to…
Added just now
Retail Store Coordinator Full time Winners - Lionhead
TJX Canada – Winners, Marshalls, HomeSense
Brampton, ON
Full-time
Support for you and your family through our Associate and Family Assistance programs, offering helpful resources and services to enhance your well-being.
Added just now
GARAGE - Seasonal Sales Associate - Oshawa Centre
Groupe Dynamite, Inc Garage
Oshawa, ON
Part-time
Reporting to the Store Manager, you’ll be the face of our brand. As a Seasonal Sales Associate, your focus is creating an elevated shopping experience - whether it’s styling customers in…
Added just now
GARAGE - Operations Associate FT - Carrefour Laval
Groupe Dynamite, Inc Garage
Laval, QC
Full-time
Reporting to the Store Manager, your role as Operations Associate is all about keeping the store flowing and the vibe strong. You’ll own the stockroom, keep inventory moving, process…
Added just now
GARAGE - Seasonal Sales Associate - Place Rosemere
Groupe Dynamite, Inc Garage
Rosemère, QC
Part-time
Reporting to the Store Manager, you’ll be the face of our brand. As a Seasonal Sales Associate, your focus is creating an elevated shopping experience - whether it’s styling customers in…
Added just now
GARAGE - Sales Associate FT - Carrefour Laval
Groupe Dynamite, Inc Garage
Laval, QC
Full-time
Reporting to the Store Manager, you’ll be the face of our brand. As a Sales Associate, your focus is creating an elevated shopping experience - whether it’s styling customers in their new…
Added just now
DYNAMITE - Seasonal Sales Associate - Sherway Gardens
Groupe Dynamite, Inc Garage
Toronto, ON · Etobicoke, Ontario
Part-time
Reporting to the Store Manager, your main focus as Seasonal Sales Associate is to provide an exceptional shopping experience to each customer, and build long term relationships with each…
Added just now
GARAGE - Seasonal Sales Associate - Galeries Terrebonne
Groupe Dynamite, Inc Garage
Terrebonne, QC
Part-time
Reporting to the Store Manager, you’ll be the face of our brand. As a Seasonal Sales Associate, your focus is creating an elevated shopping experience - whether it’s styling customers in…
Added just now
GARAGE - Sales Associate PT - Place Rosemere
Groupe Dynamite, Inc Garage
Rosemère, QC
Part-time
Reporting to the Store Manager, you’ll be the face of our brand. As a Sales Associate, your focus is creating an elevated shopping experience - whether it’s styling customers in their new…
Added just now
DYNAMITE - Seasonal Sales Associate - Bayshore Shopping Centre
Groupe Dynamite, Inc Garage
Ottawa, ON · Nepean, Ontario
Part-time
Reporting to the Store Manager, your main focus as Seasonal Sales Associate is to provide an exceptional shopping experience to each customer, and build long term relationships with each…
Added 16 mins ago
Resident Senior Steam Turbine Mechanical Technical Advisor (TFA) - Darlington
GE Vernova
Canada
Full-time
…minimum of 10 years of experience in a customer-facing role OR an associate degree and a minimum of 15 years of experience in a customer-facing…
Added 30 mins ago
(CAN) OMNI Customer Fulfillment Associate
Walmart Canada
Estevan, SK
Full-time
Position Summary...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…
Added 30 mins ago
Clinical Research Associate
ICON Strategic Solutions
Canada
Full-time
Senior Clinical Research Associate - Vancouver
Added 30 mins ago
Clinical Research Associate
ICON Strategic Solutions
Canada
Full-time
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Added 30 mins ago
(CAN) Overnight Associate
Walmart Canada
Red Deer, AB
Contract
…processing of merchandise all in a safe and clean environment. This Associate will function as part of a team to strategically plan and execute duties based on workload and operational…
Added 30 mins ago
(CAN) OMNI Customer Fulfillment Associate
Walmart Canada
Surrey, BC
Full-time
Position Summary...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…
Added 30 mins ago
(CAN) Front End Checkout Team Associate
Walmart Canada
Nanaimo, BC
Full-time
Added 30 mins ago
(CAN) Directs Store Delivery Associate
Walmart Canada
Langley (District), BC · Langley, BC
Full-time
Works closely with the Operations Manager and Office Support Associate to identify and resolve receiving issues or discrepancies efficiently.
Added 30 mins ago
(CAN) Asset Protection Associate
Walmart Canada
Tsawwassen, BC
Full-time
Position Summary...The Asset Protection Associate plays a key role in creating and maintaining a safe, secure, and professional store environment for customers, associates, visitors, and…
Added 30 mins ago
(CAN) OMNI Customer Fulfillment Associate
Walmart Canada
Port Coquitlam, BC
Full-time
Position Summary...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…
Added 30 mins ago
(CAN) Self Checkout Attendant
Walmart Canada
Coquitlam, BC
Full-time
…opportunity to build valuable skills in customer service and retail operations. The Self‑Checkout Attendant supports a positive shopping experience by providing friendly, helpful service…
Added 30 mins ago
Pharmacy Assistant
Walmart Canada
Hamilton, ON · Waterdown, ON
Full-time
…Assistant is expected to participate in all aspects of Pharmacy Operations required of a team player. They are a key member in the delivery of superior customer…
Added 30 mins ago
Pharmacy Assistant
Walmart Canada
Port Perry, ON
Full-time
…Assistant is expected to participate in all aspects of Pharmacy Operations required of a team player. They are a key member in the delivery of superior customer…

ICON Strategic Solutions

Clinical Research Associate

Canada

Job type: Full-time
Posting language: English · French
Posted: Oct 1, 2026

Apply About employer

Applications open in a new tab.

Original job description

English section of this bilingual listing.

Clinical Research Associate - GTA

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 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 the GTA area that will monitor respiratory and CV 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) – Région du Grand Toronto (GTA)

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 - GTA

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 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 the GTA area that will monitor respiratory and CV 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) – Région du Grand Toronto (GTA)

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 recherchons un(e) CRA dans la région du Grand Toronto (GTA) pour assurer le suivi d’études en respiratoire et en cardiovasculaire.

Ce que vous ferez

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

Principales Responsabilités

Assurer le suivi des sites d’essais cliniques afin de garantir le respect des protocoles d’étude, des exigences réglementaires et des normes de Bonnes Pratiques Cliniques (BPC/GCP).
Effectuer des visites sur site pour évaluer la performance des centres, résoudre les enjeux opérationnels et fournir le soutien nécessaire à la réussite des études.
Collaborer avec des équipes multidisciplinaires afin d’assurer une collecte de données et une production de rapports exactes et réalisées dans les délais prescrits.
Offrir de la formation et de l’accompagnement au personnel des sites ainsi qu’aux autres ARC/CRA afin de maintenir des normes élevées de conduite des essais cliniques.
Établir et maintenir 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 une solide expérience en surveillance d’essais cliniques ainsi que la capacité de travailler de façon autonome tout en servant de mentor et de ressource auprès des autres membres de l’équipe.

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 de recherche clinique et des exigences réglementaires.
Capacité démontrée à gérer simultanément plusieurs sites et projets, avec de solides compétences en organisation et en résolution de problèmes.
Expertise en surveillance clinique, en intégrité des données et en gestion de sites, ainsi qu’une maîtrise des logiciels et outils utilisés dans le cadre des essais cliniques.
Excellentes aptitudes 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 pour 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

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, while assessing site performance and resolving operational issues. Coordinate with cross-functional teams, support accurate and timely data collection and reporting, train site staff and other CRAs, and maintain effective stakeholder relationships.

Requirements

A bachelor's degree in a relevant scientific or healthcare-related field and extensive experience as a Clinical Research Associate are required, along with strong knowledge of clinical trial processes and regulatory requirements. Candidates should be able to manage multiple sites and projects, demonstrate expertise in monitoring, data integrity, and site management, communicate effectively, use clinical trial software, and travel approximately 60%.

Skills

Clinical Trial Monitoring
Good Clinical Practice
Regulatory Compliance
Site Management
Data Integrity
Clinical Trial Operations
Site Visits
Issue Resolution
Data Collection and Reporting
Staff Training and Guidance
Stakeholder Management
Communication
Interpersonal Skills
Organization
Problem-Solving
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 Trial Monitoring
Clinical Trials
Respiratory Studies
Cardiovascular Studies
Good Clinical Practice
Regulatory Requirements
Study Protocols
Site Visits
Site Performance
Site Management
Data Integrity
Data Collection
Reporting
Clinical Trial Software
Monitoring Practices
Quality Improvement
Cross-Functional Collaboration
Stakeholder Management
Site Staff Training
Clinical Trial Operations
Multiple Site Management
Pharmaceutical Manufacturing
Travel

Report this job