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Added 2 days ago
Strategic Sourcing - Strategic Sourcing Associate
Mohawk Medbuy Corporation (MMC)
Burlington, ON · ON · Kingston, ON · London, ON · Oakville, ON · Thunder Bay, ON · Toronto, ON · Chatham-Kent, ON
We are currently recruiting for a full-time Strategic Sourcing Associate to support our IT team within our Strategic Sourcing team.
Added 2 days ago
IS
Site Activation Partner
ICON Strategic Solutions
Canada
- Full-time
As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of…
Added 2 days 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 2 days ago
IS
Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Added 2 days ago
IS
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 2 days ago
IS
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 2 days ago
AC
Administrative Associate
Aston Carter
Mississauga, ON
- $25 to $28 CAD / hour
- Contract
We are seeking a detail-oriented and customer-focused Administrative Associate to join our team. This role involves working closely with clinical trial teams across multiple countries,…
Added 2 days ago
IS
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 2 days ago
IS
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 3 days ago
A
Associate Director, Supply Chain Planning
AstraZeneca
Hamilton, ON · Canada – Hamilton – Longwood Road South
- Full-time
We are seeking a strategic and analytical Associate Director of Supply Chain Planning to lead clinical supply forecast planning and drive cross-functional alignment. In this vital…
Added 3 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (Hybrid role in Mississauga)
Added 3 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
Added 3 days ago
IP
Clinical Trial Associate
ICON plc
Burlington, ON · Canada, Burlington
- Full-time
Clinical Trial Associate (Hybrid role in Mississauga)
Added 3 days ago
IP
Clinical Trial Associate
ICON plc
Burlington, ON · Canada, Burlington
- Full-time
Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
Added 4 days ago
AP
Manager, Regulatory Affairs
Alexion Pharmaceuticals, Inc.
Mississauga, ON
- Full-time
Provide oversight of clinical trial related submissions, including CTA, CTA-Amendment and CTA-Notification to Health Canada as needed.
Added 4 days ago
J
Senior Clinical Research Associate
Jobgether
Canada
- Full-time
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Research Associate based in Canada.
Added 5 days ago
IP
Clinical Trial Associate
ICON plc
Burlington, ON · Canada, Burlington
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 5 days ago
A
Manager, Regulatory Affairs
AstraZeneca
Mississauga, ON · Canada - Mississauga
- Full-time
Provide oversight of clinical trial related submissions, including CTA, CTA-Amendment and CTA-Notification to Health Canada as needed.
Added 5 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 5 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 5 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 5 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 5 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 5 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 5 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)

ICON Strategic Solutions

Clinical Trial Associate

Burlington, ON, Canada

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

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Job details

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

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

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More about this job

Responsibilities

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

Requirements

A bachelor's degree in a scientific or healthcare-related field and at least two years of experience supporting clinical trials are required. Candidates should understand 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
Attention To Detail
Team 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
Clinical Trials
Clinical Trial Coordination
Clinical Trial Administration
Study Protocols
Regulatory Requirements
Clinical Trial Documentation
Study Files
Essential Documents
Regulatory Submissions
Informed Consent Forms
Case Report Forms
Cross-Functional Teams
Clinical Trial Metrics
Trial Milestones
Pharmaceutical Manufacturing
Sponsor-Dedicated Model

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