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Added 11 hours ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…following established governmental guidelines and regulations, the Clinical Trial Project Manager is responsible for the operational management of multicentre clinical research studies. The…
Added 19 hours ago
MM
Strategic Sourcing Associate
Mohawk Medbuy Corporation
Toronto, ON · Greater Toronto Area, Canada
- $53,736 to $62,980 CAD / year
- Full-time
We are currently recruiting for a full-time Strategic Sourcing Associate to support our Furniture, Fixtures and Equipment (FF&E) team within our Strategic Sourcing team. This role will…
Added 22 hours ago
I
Associate Director Quality Management
IQVIA
Quebec, QC
- Full-time
Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated
Added 23 hours ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…following established governmental guidelines and regulations, the Clinical Trial Project Manager is responsible for the operational management of multicentre clinical research studies. The…
Added 1 day ago
AH
Clinical Research Coordinator-Hematology
Alberta Health Services
AB · Greater Edmonton Metropolitan Area
- Temporary
Are you an experienced clinical trial professional looking to work with cutting-edge cancer therapies? We are seeking a dynamic Clinical Trials Coordinator to join our Clinical Trial Unit…
Added 1 day ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…following established governmental guidelines and regulations, the Clinical Trial Project Manager is responsible for the operational management of multicentre clinical research studies. The…
Added 1 day ago
IS
Senior Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Added 1 day ago
B
Evidence Delivery Associate/Manager, Medical Evidence Canada
Brunel
Mississauga, ON
- Full-time
Set up and maintain the study in Veeva Clinical Vault (e.g., upload files, enter information into fields, performance assessments)
Added 1 day ago
AG
Associate Intern - Health Care (HEOR, Epidemiology & Market Access)
Analysis Group
Toronto, ON
- Internship
…data, including electronic health records, insurance claims, clinical trial datasets, registries, and survey data to perform sophisticated analyses that inform client strategies in HEOR,…
Added 1 day ago
IS
Bilingual FR/EN Study Start-up CRA
ICON Strategic Solutions
Canada
- Full-time
As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.
Added 1 day ago
IS
Sr Start-up Manager
ICON Strategic Solutions
Burlington, ON
- Full-time
The Study Start-up/Site Activation Lead works in close collaboration with the CRAs and the Local Study Team/Local Study Associate Director to ensure that study start-up activities and…
Added 2 days ago
AP
Clinical Operations Manager-Traveling CRC Team
ActivMed Practices & Research, LLC.
Burlington, ON
- Full-time
…identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and…
Added 2 days ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…following established governmental guidelines and regulations, the Clinical Trial Project Manager is responsible for the operational management of multicentre clinical research studies. The…
Added 3 days ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…following established governmental guidelines and regulations, the Clinical Trial Project Manager is responsible for the operational management of multicentre clinical research studies. The…
Added 5 days ago
IS
Sr. Site Management Assoociate
ICON San Antonio
Montreal, QC
- Full-time
Sr. Site Management Associate (French Speaking)
Added 5 days ago
MC
Associate Director, Clinical Data Management
Merck Canada
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
The Associate Director, Data Collection Data Steward, Global Data Management and Standards (GDMS), Global Clinical Data Standards (GCDS) provides program-level oversight of data standards,…
Added 5 days ago
S
Clinical Research Associate I (SRI) - Odette Cancer Centre Clinical Trials - Temporary Full-Time 2026-19105 (2026-19105)
Sunnybrook
Toronto, ON
- Full-time
Applying clinical trial protocol requirements into patient & data activities such as documenting medical history, medications and adverse events from patients; reporting Serious Adverse…
Added 5 days ago
G
Clinical Study Associate
GSK
Mississauga, ON
- Full-time
- Support site feasibility activities by researching potential clinical trial sites and compiling results for studies in Canada.
Added 6 days ago
S
Clinical Research Associate I (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-19096 (2026-19096)
Sunnybrook
Toronto, ON
- Full-time
Applying clinical trial protocol requirements into patient & data activities such as documenting medical history, medications and adverse events from patients; reporting Serious Adverse…
Added 6 days ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…following established governmental guidelines and regulations, the Clinical Trial Project Manager is responsible for the operational management of multicentre clinical research studies. The…
Added 6 days ago
NS
Research Coordinator Non-Clinical - APMPM - Department of Research
Nova Scotia Health Authority
Halifax, NS
- Full-time
Knowledge of medical terminology and clinical trial regulatory guidelines
Added 6 days ago
A
Clinical Research Associate I
AbbVie
Edmonton, AB
- Full-time
Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.
Added 6 days ago
NN
Sr. Clinical Research Associate
Novo Nordisk
Montreal, QC
- Full-time
Added 6 days ago
Research Coordinator Non-Clinical - APMPM - Department of Research
Nova Scotia Health and IWK Health
Halifax, NS
Knowledge of medical terminology and clinical trial regulatory guidelines
Added 7 days ago
G
Medical Science Liaison, Hepatology –Alberta/Saskatchewan
GSK
Regina, SK · Saskatoon, SK · Calgary, AB · Field Worker - CAN
- Full-time
Experience presenting and contextualizing complex clinical trial data and publications to clinicians in hepatology or related therapeutic areas (e.g., chronic hepatitis B, liver disease).

ICON Strategic Solutions

Senior 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.

Senior 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 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 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

Senior 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 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 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 resolving issues and supporting trial execution. Collaborate with cross-functional teams, support accurate and timely data collection and reporting, and train site staff and other CRAs.

Requirements

Requires a bachelor's degree in a relevant scientific or healthcare-related field and extensive Clinical Research Associate experience with a strong understanding 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, and travel approximately 60%.

Skills

Clinical Trial Monitoring
Good Clinical Practice
Regulatory Compliance
Site Management
Data Integrity
Clinical Trial Protocols
Site Visits
Clinical Data Collection
Clinical Reporting
Stakeholder Management
Cross-Functional Collaboration
Training and Mentoring
Problem-Solving
Organizational Skills
Clinical Trial Software
Respiratory and Cardiovascular Studies

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
Good Clinical Practice
Regulatory Requirements
Clinical Trial Protocols
Site Visits
Site Performance
Site Management
Data Integrity
Clinical Data Collection
Clinical Reporting
Respiratory Studies
Cardiovascular Studies
Clinical Trial Software
Monitoring Practices
Stakeholder Management
Cross-Functional Teams
Quality Improvement
Clinical Trial Compliance
Travel

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