About the role

Clinical Research Associate monitoring respiratory and cardiovascular trials for ICON’s sponsor-dedicated clinical research operations. Managing GTA sites, compliance, data integrity, and trial execution.

Responsibilities

Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
Lead clinical trial monitoring tasks with a focus on quality and continuous improvement
Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
Conduct site visits to assess site performance, resolve issues, and provide support
Collaborate with cross-functional teams on timely and accurate data collection and reporting
Provide training and guidance to site staff and other CRAs
Build and maintain relationships with site personnel and stakeholders
Monitor respiratory and cardiovascular studies in the GTA area

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management
Proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills
Ability to influence and drive compliance within a complex environment
Willingness to travel as required (approximately 60%)
Legal right to work in the country where the role is based

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