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ICON plc
ICON plc
ConsultingHealthcareLogistics
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.
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Clinical Research Associate – Respiratory and Cardiovascular Trials, Canada Remote

Monitor respiratory and cardiovascular clinical trials for ICON’s sponsor-dedicated research operations. Oversee GTA sites, compliance, data quality, and trial delivery.

CACanadaRemoteFull-timeJuniorMiddleEnglish RequiredClinical Research

Description

  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead monitoring activities with an emphasis on quality and ongoing improvement
  • Verify site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits to evaluate performance, resolve concerns, and provide operational support
  • Coordinate with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop and maintain effective relationships with site teams and key stakeholders
  • Monitor respiratory and cardiovascular studies across the GTA

Requirements

  • Bachelor’s degree in a relevant scientific discipline or healthcare-related field
  • Extensive Clinical Research Associate experience, with a strong grasp of clinical trial procedures and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects concurrently, supported by strong organizational and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management
  • Proficiency with relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management capabilities
  • Ability to influence others and promote compliance in a complex environment
  • Willingness to travel as needed, approximately 60%
  • Legal authorization to work in the country where the role is based

Benefits

  • Competitive base pay with performance-related incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension programs
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Structured training, learning, and career development opportunities

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