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Added 1 min ago
HT
IT Internal Auditor
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 1 min ago
HT
Trade Compliance Program Manager
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 1 min ago
HT
Internal Auditor (Business Control & IT)
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 1 min ago
HT
Financial Manager
Husky Technologies
Bolton, ON
- Full-time
Evaluate financial performance of new service products, metrics to drive critical business behavior as well as structures, systems and processes that lead to ease of analysis and reporting
Added 1 min ago
HT
Manager, Internal Controls
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 1 min ago
HT
Test Engineering Technologist
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 1 min ago
HT
Financial Manager - PLM (Product Line Mgmt)
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 3 mins ago
HT
VP, Accounting & Controllership (Husky)
Husky Technologies
Bolton, ON
- Full-time
Lead all global accounting, financial reporting, consolidation, controllership, and financial governance activities.
Added 3 mins ago
HT
Software Validation Technologist
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 3 mins ago
HT
A/P Administrator
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 3 mins ago
HH
Research Project Manager I
Hamilton Health Sciences
Hamilton, ON
- Full-time
The Research Project Manager I is to lead a team in the conduct of one or more research studies and accountable to the Principal Investigator (PI), (Associate) Program Manager/Program…
Added 3 mins ago
Senior Engineer (Water Services)
Region of Waterloo
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Chairs/conducts public meetings and consultations as the project lead. Responds to public complaints regarding high profile/complex/politically sensitive projects.
Added 3 mins ago
B
Manager, Business Restructuring & Turnaround Services
BDO
Oakville, ON · Toronto, ON
- Full-time
…work directly with senior client and stakeholder groups, and lead and develop members of the engagement team. You will have exposure to a broad range of mandates, which may include…
Added 3 mins ago
M
Senior IT Project Manager
Manulife
Toronto, ON
- Full-time
…Data & AI teams, control functions, and external partners to lead complex, cross-functional initiatives from concept through implementation. This role engages global stakeholders across…
Added 3 mins ago
Sr Analyst Data & Analytics
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…As part of the Performance Management area, this role will lead complex data management, analysis, and reporting work for the department. The Senior Data Analyst will translate business…
Added 18 mins ago
Senior Manager, Integrated Marketing (Masterbrand)
Sephora
Toronto, ON
…strategies and campaigns. The work you do will impact beauty, as you lead category, gifting, and promotional campaigns that bring Sephora’s differentiators to life. You’ll manage a team of…
Added 32 mins ago
C
Associate Golf Course Superintendent - RattleSnake Point Golf Club
ClubLink
Milton, ON
- Full-time
Reporting directly to the Golf Course Superintendent, the Associate Golf Course Superintendent plays a key leadership role in the day-to-day management and maintenance of the golf course.…
Added 48 mins ago
M
Senior Manager, Indigenous Audit
MNP
Abbotsford, BC · Chilliwack, BC · Vancouver, BC · BC · Surrey, BC
- Full-time
Lead client facing engagement teams to complete audits, compliance tax engagements, budgeting, internal controls, and financial/accounting transactions
Added 1 hour ago
SS
Campus Security Supervisor - Kelowna
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- Full-time
Train, mentor, and coach officers on site duties, protocols, reporting standards, and company policies
Added 1 hour ago
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Senior Interior Designer - Team Lead
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…urgently seeking a seasoned Senior Interior Designer: Team Lead Interior Designer. The firm has expertise in large scale residential projects with multiple stakeholders; & seek an Interior…
Added 1 hour ago
SI
Automation Controls Lead
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- Full-time
Saputo is seeking an Automation Controls Lead, for an existing opportunity within our organization. Reporting to the Maintenance Manager, this position specializes in automation, control…
Added 1 hour ago
RO
Assistant Manager, Retail In-store Sales & Service (12-month Contract)
Royal Ontario Museum
Toronto, ON
- Contract
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Added 1 hour ago
EA
Mechanical Production Project Lead / Lead Millwright
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- Full-time
Reporting to the Mechanical Production Supervisors, the Mechanical Production Project Lead will provide leadership and coordination of mechanical manufacture of the project. The incumbent…
Added 1 hour ago
RB
Regional Coordinator
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Vaughan, ON
- Full-time
Lead regional marketing and partnering efforts through website management, powerpoint presentations, reporting, workshop coordination, community engagement facilitation and, strategy support
Added 1 hour ago
KD
Représentant, Ventes de territoire | Territory Sales Representative
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Quebec, QC
- Full-time
…for managing assigned stores within the province of Quebec. Reporting into the Regional Field Sales Lead, the TSR is accountable for driving distribution and display of KDP products, the…

ICON Strategic Solutions

Clinical Research Associate

Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English · French
Posted: Oct 2, 2026

Original job description

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.

Job Advert Posting

As a CRA II 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%)

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.

Job Advert Posting

As a CRA II 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 CRA experience with a strong understanding of clinical trial processes and regulatory requirements are required. Candidates should be able to manage multiple sites and projects, demonstrate expertise in monitoring, data integrity, and site management, communicate effectively, and travel approximately 60%.

Skills

Clinical Trial Monitoring
Good Clinical Practice
Regulatory Compliance
Site Management
Data Integrity
Clinical Trial Operations
Site Performance Assessment
Issue Resolution
Data Collection and Reporting
Cross-Functional Collaboration
Staff Training and Guidance
Stakeholder Management
Organization
Problem-Solving
Clinical Trial Software
Communication

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
CRA II
Senior CRA
Clinical Trials
Clinical Trial Monitoring
Good Clinical Practice
Regulatory Requirements
Study Protocols
Site Visits
Site Performance
Site Management
Data Integrity
Data Collection
Clinical Trial Reporting
Clinical Trial Software
Respiratory Studies
Cardiovascular Studies
Quality Improvement
Cross-Functional Teams
Stakeholder Management
Site Staff Training
Pharmaceutical Manufacturing

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