Full-time jobs in Canada

Explore full-time jobs across Canada. Choose a location and read the full job details.

195,213 listings · 20,431 employers Counted Sep 22, 2026. How we count

About these jobs

Employers hiring include Walmart Canada (4,775 listings), Starbucks Coffee Company (1,947 listings), Loblaw Companies Limited (1,766 listings).

Common roles: Project manager, Sales representative, Store manager.

21,332 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / year	80,000.00	12,285
CAD / hour	23.55	6,308
USD / year	95,710.00	1,094
USD / hour	21.00	413
CAD / month	5,764.00	265
CAD / week	850.00	29
USD / month	5,000.00	19
GBP / hour	35.00	16
GBP / year	40,000.00	14
CAD / day	367.50	12

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 2% remote, 18% hybrid, 80% on-site, 0% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Full-time jobs in Canada

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ICON Strategic Solutions

Study Start Up Associate

Canada

Job type: Full-time
Posting language: English
Posted: Sep 21, 2026

Apply About employer

Applications open in a new tab.

Original job description

Site Activation Partner

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 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 innovative treatments and therapies.

What You Will Do

Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders.

Key Responsibilities Include

Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
Maintaining accurate and up-to-date records of regulatory submissions and approvals.
Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.
Participating in study start-up meetings and providing input on regulatory requirements and timelines.

Your Profile

You will bring relevant site start-up and activation experience, along with the following qualifications and skills.

Required Qualifications And Experience

Bachelor's degree in life sciences or a related field.
Previous experience in clinical research or regulatory affairs preferred, but Nt required.
Strong attention to detail and organizational skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.
Willingness to travel as required (approximately 5%)

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

The Study Start Up Associate facilitates the initiation of clinical trials by preparing regulatory documents and coordinating with stakeholders. They ensure compliance with regulatory requirements and maintain accurate records throughout the study start-up process.

Requirements

Candidates must hold a bachelor's degree in life sciences or a related field. Strong organizational skills and the ability to manage multiple tasks in a fast-paced environment are required.

Skills

Clinical trials
Regulatory compliance
Site activation
Regulatory submissions
Ethics committee submissions
Clinical research
Regulatory affairs
Attention to detail
Organizational skills
Communication skills
Interpersonal skills
Cross-functional collaboration
Protocol development
Informed consent forms
Investigator brochures

Benefits

Annual leave entitlements
Health insurance
Retirement planning
Global 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
Site activation
Regulatory affairs
Life sciences
Clinical research
Regulatory submissions
Ethics committee
Protocol
Informed consent
Investigator brochure
Pharmaceutical manufacturing
Compliance
Stakeholder management
FSP organization

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