Jobs in Canada

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Added 1 hour ago
J
Senior Clinical Trial Manager (Sr CTM), Dermatology & Rheumatology
Jobgether
Canada
- Full-time
The Senior Clinical Trial Manager will oversee clinical trial operations and monitoring activities across dermatology and rheumatology studies, ensuring high-quality delivery and compliance…
Added 3 hours ago
TU
Research Associate
The University of British Columbia
Kelowna, BC
- Full-time
The Research Associate develops collaborations across both UBC campuses, including the Michael Smith Laboratories (MSL), and with clinical, government and industry partners. Working with…
Added 5 hours ago
H
Clinical Research Site Supervisor
HealthCareersInSask.ca
Regina, SK
- Full-time
The Clinical Research Site Supervisor is actively involved in supporting quality assurance and quality improvement activities in the department, which would include; monitoring compliance…
Added 7 hours ago
UO
Research Associate
University of British Columbia
Kelowna, BC · UBCO | Engineering, Management and Education Building (EME)
- Full-time
The Research Associate develops collaborations across both UBC campuses, including the Michael Smith Laboratories (MSL), and with clinical, government and industry partners. Working with…
Added 12 hours ago
I
Consultant, Services de conseil et d’analyse / Consultant, Consulting & Analytics Services
IQVIA
Mississauga, ON · Montreal, QC · Quebec, QC
- Full-time
Participer à des interactions clients (p. ex., appels, ateliers) pour clarifier les besoins, tester des hypothèses et expliquer les méthodes, avec soutien de l’équipe senior.
Added 12 hours ago
Research Associate (Limited Term, 2 years)
University of Toronto
Toronto, ON
The Research Associate will serve as a senior scientific leader within the lab and will work in close partnership with Dr. Bowen Li (Principal Investigator) to oversee and advance the lab’s…
Added 21 hours ago
Associate Principal/Strategy & Medical Affairs (Life Sciences)
Charles River Associates - Private
Toronto, ON
…organizations, and advocacy groups from the earliest stages of research into new therapy areas, through clinical development, to the launch of therapies that will achieve commercial success…
Added 22 hours ago
UO
Senior Advisor, Executive Operations
University of Ottawa
Ottawa, ON · Roger Guindon Hall
- Full-time
…supported in carrying out institutional, Faculty, academic, research, clinical partnership and external leadership responsibilities. Establishes and maintains effective communication…
Added 1 day ago
UH
Technical Specialist
University Health Network
Toronto, ON
- Full-time
The Technical Specialist work closely with other Business Intelligence (BI) Analyst and Developer, Data Engineers, Clinical/SME teams and Other Epic Application Team, this position is…
Added 1 day ago
UH
Project Coordinator I - Peter Munk Cardiac Centre - Quality Registry
University Health Network
Toronto, ON
- Full-time
…Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international…
Added 1 day ago
UH
Project Coordinator I - Peter Munk Cardiac Centre - Quality Registry
University Health Network
Toronto, ON
- Full-time
…Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international…
Added 2 days ago
IP
Associate Clinical System Designer
ICON plc
Burlington, ON · Canada, Burlington
- Full-time
Associate Clinical System Designer - United States, Canada, Mexico, Colombia
Added 2 days ago
P(
Associate Creative Strategist
Phoenix (YC W21)
Toronto, ON
- $70,000 to $80,000 CAD / year
- Full-time
We’re looking for an Associate Creative Strategist to help us scale performance creative across both of our brands, Phoenix and Raven. This is a hands-on, apprenticeship-style role for…
Added 2 days ago
I
Directeur adjoint, Solutions et pres associée, Stratégie des solutions et prestation (SDL) / Associate Director, Solution and Delivery Lead (SDL)
IQVIA
Toronto, ON
- Full-time
The Associate Director, Solution and Delivery Lead (SDL) serves as a strategic, scientific, and delivery leader within Real World Evidence (RWE) Solutions. This role is accountable for…
Added 2 days ago
IS
Clinical Research Associate 3
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 2 days ago
PC
Senior Clinical Research Associate
PSI CRO
Calgary, AB
- $120,000 to $150,000 CAD / year
- Full-time
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality…
Added 3 days ago
SH
Skin Wellness Associate Nurse
SE Health
Mississauga, ON
- Full-time
…the way we do our work. As a social enterprise, we support research into Senior’s Health and…
Added 3 days ago
TU
Senior Research Analyst, Pharmacoepidemiology
The University of British Columbia
Victoria, BC
- $8,087.08 to $12,117.08 CAD / month
- Full-time
The Senior Research Analyst will manage a team of research analysts and data analysts to perform pharmacoepidemiology studies for the BC Ministry of Health (MoH), Canadian Network for…
Added 3 days ago
P
Associate Creative Strategist
Phoenix
Toronto, ON
- $70,000 to $80,000 CAD / year
- Full-time
We’re looking for an Associate Creative Strategist to help us scale performance creative across both of our brands, Phoenix and Raven. This is a hands-on, apprenticeship-style role for…
Added 3 days 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
The Senior Research Analyst will manage a team of research analysts and data analysts to perform pharmacoepidemiology studies for the BC Ministry of Health (MoH), Canadian Network for…
Added 3 days ago
AP
Senior Medical Science Liaison Hematology/Oncology (Ontario West/Manitoba)
Astellas Pharma
Markham, ON
- Full-time
Astellas Canada – Senior Medical Science Liaison Hematology/Oncology (Ontario West/Manitoba)
Added 3 days ago
Scientific Director - Geriatric Division Research
CAMH
Toronto, ON
As Canada’s leading mental illness research facility, CAMH’s Campbell Family Mental Health Research Institute (CFMHRI) is home to scientists, staff and research trainees conducting leading…
Added 3 days ago
QU
Faculty Resource & Compensation Coordinator (J0926-0129)
Queen's University
Kingston, ON
- $62,142 to $75,772 CAD / year
- Full-time
Reporting to the Associate Director, Administration, Initiatives, and Operations (AIO), the Faculty Support Coordinator performs a broad range of complex administrative, operational, and…
Added 3 days ago
Associate Director of Programs - Wellbrook Place West
Partners Community Health
Mississauga, ON
Identify service gaps and emerging resident needs, and lead the design of new or enhanced programs in collaboration with clinical and interdisciplinary teams.
Added 3 days ago
ASSOCIATE SCIENTIST I - AGS
DiaSorin
Toronto, ON
Participate in the Company's day-to-day Research and Development activities which include: design, execution and interpretation of scientific experiments and design and development of…

ICON Strategic Solutions

Clinical Research Associate 3

Canada

Full-time

Apply on LinkedIn About employer

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Job details

Job type: Full-time
Posting language: English
Posted: Nov 10, 2026

Original job description

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.

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

Apply on LinkedIn 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 performance and resolving issues. Coordinate with cross-functional teams, support accurate data collection and reporting, train site staff and other CRAs, and maintain effective stakeholder relationships.

Requirements

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

Skills

Clinical Trial Monitoring
Good Clinical Practice
Regulatory Compliance
Site Management
Clinical Trial Protocol Adherence
Site Visits
Issue Resolution
Data Integrity
Data Collection and Reporting
Clinical Trial Software
Training and Guidance
Stakeholder Management
Communication
Organizational Skills
Problem-Solving
Cross-Functional Collaboration

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
Good Clinical Practice
Regulatory Requirements
Study Protocols
Site Visits
Site Performance
Site Management
Data Integrity
Data Collection
Data Reporting
Clinical Trial Software
Monitoring Practices
Cross-Functional Teams
Stakeholder Management
Clinical Trial Conduct
Quality Improvement
Pharmaceutical Manufacturing
Sponsor-Dedicated Model

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Work requirements

Jobs in Canada