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Added 4 hours ago
Strategic Sourcing - Strategic Sourcing Associate
Mohawk Medbuy Corporation (MMC)
ON · Thunder Bay, ON · Kingston, ON · London, ON · Toronto, ON · Oakville, ON · Burlington, ON · Chatham-Kent, ON
We are currently recruiting for a full-time Strategic Sourcing Associate to support our Cardiac team within our Strategic Sourcing team.
Added 11 hours ago
A
Screening Quality Control Associate I
Altasciences
Montreal, QC
- Full-time
The Screening Quality Control Associate I is responsible for ensuring the accuracy, completeness, and compliance of all data collected during the screening phase of clinical trials. This…
Added 1 day ago
ML
Senior CRA
Meet Life Sciences
Canada
- Contract
Seeking an experienced, French-speaking Senior Clinical Research Associate (CRA) to support clinical trial monitoring, site management, regulatory documentation, and budget negotiations for…
Added 4 days ago
AH
Clinical Research Coordinator - Phase 1 Group
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 4 days ago
Strategic Sourcing - Strategic Sourcing Associate
Mohawk Medbuy Corporation (MMC)
Burlington, ON · Toronto, ON
We are currently recruiting for a full-time Strategic Sourcing Associate to support our Indirect Spend (Facilities Management, Professional Services, IT) team within our Strategic Sourcing…
Added 5 days ago
IS
Sr. Site Management Assoociate
ICON Strategic Solutions
Canada
- Full-time
As a Senior Site Management Associate at ICON, you will oversee site management activities, ensuring the smooth operation of clinical trials at the site level.
Added 5 days ago
XP
Research Associate 1 or 2, Biology (12 Month Contract)
Xenon Pharmaceuticals
Burnaby, BC
- $58,100 to $81,000 CAD / year
- Full-time
…clinically validated potassium channel modulator in late-stage clinical development for multiple indications. In March 2026, we announced positive topline data from our Phase 3 X-TOLE2…
Added 5 days ago
IS
Bilingual Senior Site Management Associate (French-speaking)
ICON Strategic Solutions
Canada
- Full-time
As a Senior Site Management Associate at ICON, you will oversee site management activities, ensuring the smooth operation of clinical trials at the site level.
Added 6 days ago
NS
Research Coordinator (Registered Nurse) - Hematology Research
Nova Scotia Health Authority
Halifax, NS
- Full-time
Reporting to the Associate Director and Manager, Hematology Research, the Research Coordinator RN is responsible for the coordination of research projects conducted at QEII within the…
Added 7 days ago
EL
Regulatory Associate/Sr Regulatory Associate /Manager, GRA, Canada affiliate
Eli Lilly and Company
ON · Ontario, Canada
- Full-time
Regulatory Associate/Sr Regulatory Associate /Manager, GRA, Canada
Added 7 days ago
Strategic Sourcing - Strategic Sourcing Associate
Mohawk Medbuy Corporation (MMC)
ON · Thunder Bay, ON · Kingston, ON · London, ON · Toronto, ON · Oakville, ON · Burlington, ON · Chatham-Kent, ON
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.
Added 10 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 11 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 11 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 11 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 11 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 11 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 11 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 11 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 13 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 14 days ago
IS
Clinical Study Associate (Hybrid - Mississauga)
ICON Strategic Solutions
Mississauga, ON
- Full-time
Clinical Trial Associate (hybrid - home/office based in Mississauga)
Added 14 days ago
NS
Licensed Research Coordinator (LPN) - Urology Research - Department of Research
Nova Scotia Health Authority
Halifax, NS
- Full-time
CCRP (Certified Clinical Research Professional) or CCRA (Certified Clinical Research Associate) an asset
Added 14 days ago
PH
Clinical Trials Nurse Coordinator
Provincial Health Services Authority
Surrey, BC
- Part-time
Coordinate the treatment programs of clinical trial patients, in collaboration with other members of the Clinical Trials Team, by preparing sample preprinted orders that reflect the patient…
Added 14 days ago
PH
Clinical Trials Nurse Coordinator
Provincial Health Services Authority
Vancouver, BC
- Full-time
Coordinate the treatment programs of clinical trial patients, in collaboration with other members of the Clinical Trials Team, by preparing sample preprinted orders that reflect the patient…
Added 15 days ago
AG
Summer Research Professional Intern-Health Care (HEOR, Epidemiology & Market Access) -Montreal/Toronto (2027 Start Date) | Stage d’été-Professionnel de recherche-Économie de la santé, biostatistique, et épidémiologie - Montréal/Toronto (Date de début 2027)
Analysis Group, Inc.
Toronto, ON · Montreal, QC
- Other
…sources - including electronic health records, claims data, clinical trial data, registries, and survey data - using statistical tools such as R, SAS, Stata, and…

Closed listing

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

This opening has closed.

The original listing is kept below for reference.

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About employer

Job details

Pay: Pay Range ($55,000 – $67,000 CAD) - Actual salary will be based on experience
Job type: Full-time
Closing date: Oct 31, 2026
Posting language: English
Posted: Oct 1, 2026

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Original job description

Archived listing. The details below describe a past opening.

Clinical Trial Associate (Hybrid role 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

About employer

More about this job

Responsibilities

Coordinate and administer clinical trials while maintaining study files, essential documents, and regulatory submissions in compliance with protocols and requirements. 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
Clinical Trial Documentation
Regulatory Documentation
Regulatory Compliance
Clinical Trial Processes
Clinical Research
Informed Consent Forms
Case Report Forms
Cross-Functional Communication
Clinical Trial Metrics Tracking
Milestone Reporting
Organization
Communication
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 Trials
Clinical Research
Clinical Trial Coordination
Clinical Trial Administration
Study Files
Essential Documents
Regulatory Submissions
Regulatory Documentation
Regulatory Requirements
Clinical Trial Protocols
Informed Consent Forms
Case Report Forms
Trial Metrics
Trial Milestones
Cross-Functional Teams
Pharmaceutical Manufacturing
Sponsor-Dedicated Model

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