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ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
Clinical Research Associate – Canada Remote | ICON plc
Monitor respiratory and cardiovascular clinical trials for ICON Strategic Solutions across Canada's Greater Toronto Area. Coordinate site visits, compliance, data quality, and guidance for clinical research teams.
Description
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Drive monitoring activities focused on quality and ongoing process improvement
- Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
- Complete site visits to review performance, address issues, and support effective study delivery
- Partner with cross-functional teams to ensure accurate, timely data collection and reporting
- Train and advise site staff and fellow Clinical Research Associates
- Develop and sustain productive relationships with site teams and other stakeholders
- Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area
Requirements
- Bachelor's degree in a relevant scientific or healthcare discipline
- Extensive Clinical Research Associate experience with a strong grasp of clinical trial operations and regulatory obligations
- Demonstrated ability to oversee multiple sites and projects concurrently
- Strong planning, organization, and problem-solving capabilities
- Advanced knowledge of monitoring methods, data integrity, and site management
- Proficiency with applicable clinical trial software and tools
- Highly effective communication, interpersonal, and stakeholder management skills
- Ability to influence others and promote compliance in a complex setting
- Availability to travel as needed, approximately 60%
- Legal authorization to work in the country where the position is based
Benefits
- Competitive base pay with performance-based incentives
- Health and wellness programs, including medical, dental, and vision coverage where available
- Retirement and pension provisions
- Life insurance and disability protection
- Employee assistance programs and wellbeing resources
- Structured training, professional development, and career progression opportunities
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