Jobs in Canada

25+ jobs

Email me new jobs Save this search

Added 12 mins ago
Senior Account Manager, Special Loans and Restructuring
EQ Bank | Canada's Challenger Bank
Toronto, ON
Full-time
…services from banking and lending, to trust and credit union…
Added 42 mins ago
External Audit - Senior Associate - B&CM
Pwc UK
London, ON
Full-time
As a Senior Associate, you’ll gain in-depth knowledge into how businesses run, gain direct access to internal stakeholders and clients and work with an unrivalled range of organisations we…
Added 42 mins ago
Warehouse Associate
REXEL
Belleville, ON
$45,000 to $55,000 CAD / year
Full-time
…branches and 27000 employees. We provide innovative electrical solutions and equipment for the industrial, residential and commercial sectors. As the energy evolves, our business is…
Added 1 hour ago
District Manager Operations - Collections (GTA)
Waste Management, Inc. (WM)
Toronto, ON
Full-time
Manages the day-to-day collection operations of a single site or multiple sites or a single Line of Business or multiple Lines of Business, establishes, and maintains performance and…
Added 1 hour ago
Associate, Entertainment Banking
CIBC
Toronto, ON
Full-time
CIBC Entertainment Banking provides advisory services and tailored financial solutions to media and entertainment companies across North America. Our team is composed of specialized…
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 1 hour ago
Associé(e), Surveillance Environnementale - Quart de nuit (23h45 to 07h45) / Associate, Environmental Monitoring – Night Shift (23h45 to 07h45)
Jubilant Pharma Limited
Montreal, QC
Full-time
…famille Jubilant Pharma. Pour plus d’information, visitez le site www.jublhs.com…
Added 1 hour ago
Associate Registrar and Director of Admissions
University of Manitoba
Winnipeg, MB
$80,965.47 to $145,737.84 CAD / year
Full-time
…through technology and is passionate about building practical solutions that improve efficiency, collaboration, and service…
Added 2 hours ago
Clinical Study Associate (Hybrid - Mississauga)
ICON Strategic Solutions
Mississauga, ON
Full-time
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…
Added 2 hours ago
Management Trainee
Jobbe
Yarmouth Indian Reserve No. 33, NS · Yarmouth, NS
Full-time
Enterprise Mobility is a leading provider of mobility solutions, owning and operating the Enterprise Rent-A-Car, National Car Rental and Alamo Rent A Car brands through its integrated…
Added 3 hours ago
Building Operator
ISS
Coquitlam, BC
$30 to $45 CAD / hour
The role is responsible for identifying and delivering corrective maintenance solutions, while also performing preventive maintenance activities and scheduled inspections to ensure all…
Added 3 hours ago
Video Conference Support Engineer - ITS3
Minnesota Direct Care and Treatment
Saint-Paul, NB · St.-Paul, NB
Full-time
…documentation, and service restoration for video conferencing solutions, helping the DOC and partner agencies successfully deliver meetings, hearings, and large-scale virtual…
Added 4 hours ago
Senior Manager, Managed Asset Program (12 month contract)
Scotiabank
Toronto, ON
Contract
Contributes to the overall success of the Managed Portfolio Program Global Portfolio Solutions / Scotia Wealth Management in Canada ensuring specific individual goals, plans, initiatives…

ICON Strategic Solutions

Clinical Trial Associate

Burlington, ON, Canada

Pay: Pay Range ($55,000 – $67,000 CAD) - Actual salary will be based on experience
Job type: Full-time
Apply by: Oct 29, 2026
Posting language: English
Posted: Sep 29, 2026

Apply About employer

Applications open in a new tab.

Original job description

Clinical Trial Associate (hybrid - home/office based in Mississauga)

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.

What You Will Do

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key Responsibilities Include

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
Support the preparation of study-related materials, such as informed consent forms and case report forms.
Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your Profile

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required Qualifications And Experience

Bachelor's degree in a scientific or healthcare-related field.
A minimum of two years of experience supporting clinical trials
Knowledge of clinical trial processes, regulations, and guidelines.
Excellent organizational and communication skills.
Ability to work collaboratively in a fast-paced environment with attention to detail.
Experience managing regulatory documentation for clinical trials
Willingness to report to the Mississauga office 3 days per week

Pay Range ($55,000 – $67,000 CAD) - Actual salary will be based on experience

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

Coordinate and administer clinical trials in compliance with study protocols and regulatory requirements, maintaining study files, essential documents, and regulatory submissions. Prepare study materials, collaborate with cross-functional teams, and track and report trial metrics and milestones.

Requirements

Requires a bachelor's degree in a scientific or healthcare-related field and at least two years of experience supporting clinical trials. Candidates should know clinical trial processes, regulations, and guidelines, have experience managing regulatory documentation, and demonstrate strong organizational, communication, collaboration, and attention-to-detail skills.

Skills

Clinical Trial Coordination
Clinical Trial Administration
Regulatory Compliance
Clinical Trial Documentation
Regulatory Submissions
Informed Consent Forms
Case Report Forms
Cross-Functional Communication
Clinical Trial Metrics Tracking
Milestone Reporting
Organization
Communication
Collaboration
Attention to Detail

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
Clinical Trials
Clinical Trial Coordination
Clinical Trial Administration
Study Protocols
Regulatory Requirements
Regulatory Compliance
Clinical Trial Documentation
Study Files
Essential Documents
Regulatory Submissions
Informed Consent Forms
Case Report Forms
Cross-Functional Teams
Trial Execution
Clinical Trial Metrics
Milestones
Pharmaceutical Manufacturing
Sponsor-Dedicated Model

Report this job