As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
En tant qu’ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en santé.

YOU ARE

We are seeking a skilled and motivated CRA who meets the following qualifications:

• Bachelor’s degree or higher in life sciences or a health-related field
• 2+ years of field-based clinical research monitoring experience within a CRO or pharmaceutical company
• Strong knowledge of ICH-GCP guidelines and clinical research regulations (Health Canada)
• Experience managing multiple protocols and working across various therapy areas (Cardiovascular, Respiratory, Renal, or Vaccines preferred)
• Familiarity with Electronic Data Capture (EDC), centralized/risk-based monitoring, and metric-based environments (preferred)
• Exceptional attention to detail, time management, and organizational skills
• Must have a valid driver’s license and access to a personal vehicle

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 maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
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, colour, 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 through the form below.
https://careers.iconplc.com/reasonable-accommodations
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.

As a Clinical Research Associate (CRA) supporting Phase I–IV clinical trials across cardiovascular, respiratory, renal, and vaccine studies, your responsibilities will include:

• Conducting site selection, initiation, monitoring, and close-out visits
• Acting as the primary liaison between investigative sites and the sponsor
• Supporting document collection, Trial Master File (TMF) maintenance, and ensuring regulatory compliance
• Ensuring adherence to study protocol, Good Clinical Practice (GCP), and regulatory requirements
• Identifying and resolving site issues, managing data queries, and supporting database lock
• Providing feedback on site performance to inform future site selection
• Managing 3–5 protocols and overseeing 12–17 sites concurrently; subject to change per business needs
• This is a remote role open to candidates based in British Columbia or Alberta, with regional travel across Western Canada required.