IT Talent Acquisition Specialist
Artemys
Recruit IT infrastructure professionals for Artemys, a digital transformation company. Lead sourcing and hiring while contributing to employer branding initiatives.
Open
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.
Senior Clinical Research Associate - Canada Remote
ICON plc is seeking a Senior Clinical Research Associate to monitor respiratory and cardiovascular trials across the Greater Toronto Area. The role oversees site performance, regulatory compliance, data quality, and trial delivery.
Description
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Direct technically complex monitoring activities while advancing quality and continuous improvement
- Evaluate site compliance with protocols, regulations, and Good Clinical Practice (GCP) requirements
- Conduct site visits to review performance, address issues, and support effective trial delivery
- Partner with cross-functional teams to maintain accurate, timely data collection and reporting
- Train and support site personnel and fellow Clinical Research Associates
- Develop productive relationships with site teams and stakeholders to support efficient trial operations
- Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area
Requirements
- Bachelor’s degree in a relevant scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience with a strong grasp of clinical trial processes and regulatory obligations
- Demonstrated ability to oversee multiple sites and projects while applying strong organization 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, including the ability to influence compliance in complex settings
- Availability to travel as needed, approximately 60%
- Legal authorization to work in the country where the position is based
Benefits
- Base salary with performance-based incentives
- Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
- Retirement and pension programmes
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Structured training and career development opportunities
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