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Added 4 hours ago
IS
Bilingual FR/EN Study Start-up CRA
ICON Strategic Solutions
Canada
- Full-time
Added 4 hours ago
IS
Sr Start-up Manager
ICON Strategic Solutions
Burlington, ON
- Full-time
Added 4 hours ago
IS
Study Start Up CRA
ICON Strategic Solutions
Canada
- Full-time
Added 6 days ago
IS
Clinical Trial Associate
ICON Strategic Solutions
Burlington, ON
- Full-time
Added 11 days ago
IS
Bilingual Clinical Trial Coordinator - Regulatory/Finance- Montreal
ICON Strategic Solutions
Kirkland, QC
- Full-time
Added 12 days ago
IS
Site Engagement Lead
ICON Strategic Solutions
Canada
- Full-time
Added 19 days ago
IS
Sr. Site Management Assoociate
ICON Strategic Solutions
Canada
- Full-time
Added 20 days ago
IS
Bilingual Senior Site Management Associate (French-speaking)
ICON Strategic Solutions
Canada
- Full-time
Added 24 days ago
IS
CLINICAL TEAM OPERATIONS LEADERSHIP - BASE
ICON Strategic Solutions
Canada
- Full-time
Added 25 days ago
IS
Senior Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
Added 25 days ago
IS
Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
Added 25 days ago
IS
Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
Added 25 days ago
IS
Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
Added 25 days ago
IS
Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
Added 25 days ago
IS
Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time
Added 26 days ago
IS
Site Start-Up Specialist
ICON Strategic Solutions
Canada
- Full-time
Added 28 days ago
IS
Clinical Study Associate (Hybrid - Mississauga)
ICON Strategic Solutions
Mississauga, ON
- Full-time
Added 1 month ago
IS
Study Start-up Specialist
ICON Strategic Solutions
Canada
- Full-time
Added 1 month ago
IS
Oncology Study Delivery Associate (Hybrid - Mississauga)
ICON Strategic Solutions
Toronto, ON · Greater Toronto Area, Canada
- Full-time
Added 1 month ago
IS
Clinical Trial Manager
ICON Strategic Solutions
Montreal, QC
- Full-time
Added 2 months ago
IS
Investigator Contracts Lead / Site Contracts Lead
ICON Strategic Solutions
Canada
- Full-time
Added 3 months ago
IS
Clinical Trial Coordinator - Finance - Montreal, Canada
ICON Strategic Solutions
Canada
- Full-time
Added 4 months ago
IS
Clinical Research Associate
ICON Strategic Solutions
Canada
- Full-time

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ICON Strategic Solutions

Bilingual FR/EN Study Start-up CRA

Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Oct 27, 2026

Original job description

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%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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 status reports and documentation, and manage sponsor-generated queries while supporting study cost efficiency. Collaborate with sponsors, investigators, site staff, and other stakeholders, and ensure 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 relevant clinical trial monitoring experience and knowledge of ICH-GCP guidelines. Candidates should be able to review and evaluate medical data, communicate effectively in English, work well with others, and travel approximately 60% as required.

Skills

Clinical Trial Monitoring
Study Start-Up Coordination
Study Monitoring
ICH-GCP Guidelines
Medical Data Review
Regulatory Compliance
Patient Safety
Study Status Reporting
Study Documentation
Sponsor Query Management
Feasibility Studies
Clinical Investigator Collaboration
Written Communication
Verbal Communication
French-English Bilingualism

Benefits

Competitive Base Salary
Performance-Related Incentives
Medical Coverage
Dental Coverage
Vision Coverage
Retirement and Pension Plans
Life Assurance
Disability Coverage
Employee Assistance Programmes
Wellbeing Resources
Learning and Development Opportunities

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research
Clinical Trials
Clinical Trial Monitoring
Study Start-Up
Clinical Research Associate
CRA I
ICH-GCP
Medical Data
Patient Safety
Regulatory Requirements
Clinical Trial Protocols
Study Status Reports
Study Documentation
Sponsor-Generated Queries
Study Cost Efficiency
Feasibility Studies
Clinical Investigators
Site Staff
Stakeholder Collaboration
Pharmaceutical Manufacturing
Biotechnology Research
French
English

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