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ICON Strategic Solutions

Study Start Up CRA

Canada

Full-time

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Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English
Posted: Oct 27, 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 CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

What You Will Do

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

Key Responsibilities Include

Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Your Profile

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

Required Qualifications And Experience

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
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

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More about this job

Responsibilities

Coordinate study start-up and monitoring activities, maintain accurate study documentation and status reports, and manage sponsor-generated queries and study costs. Collaborate with investigators, site staff, and other stakeholders while ensuring patient safety and compliance with company procedures, protocols, and regulatory requirements.

Requirements

A university degree in medicine, science, or an equivalent field is required, along with knowledge of ICH-GCP and the ability to review and evaluate medical data. The role calls for clinical trial monitoring experience, strong English communication and interpersonal skills, and willingness to travel approximately 60%.

Skills

Clinical Trial Monitoring
Study Start-Up Coordination
Study Documentation
Study Status Reporting
Query Management
Clinical Feasibility Studies
Clinical Investigator Collaboration
Patient Safety
ICH-GCP Compliance
Regulatory Compliance
Medical Data Review
Written Communication
Verbal Communication
Time Management
Willingness to Travel

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 Monitoring
Study Start-Up
Clinical Trial Operations
ICH-GCP
Regulatory Requirements
Patient Safety
Medical Data
Study Documentation
Study Status Reports
Sponsor-Generated Queries
Feasibility Studies
Clinical Investigators
Site Staff
Clinical Programmes
Study Cost Efficiency
Protocol Compliance
Stakeholder Collaboration

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