Clinical Research Associate monitoring Canadian clinical trials for Parexel, a global clinical research organization. Managing site relationships, compliance, data quality, and study delivery.
About the role
- Senior Clinical Research Associate monitoring cardiovascular and respiratory clinical trials for ICON in Quebec. Ensuring site compliance, data integrity, and protocol adherence across studies.
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 (GCP) standards
- Conduct site visits to assess performance, resolve issues, and support successful trial execution
- Collaborate with cross-functional teams to ensure 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 cardiovascular and respiratory studies in Quebec
Requirements
- 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, with proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills, with the 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
Benefits
- 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
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
Report this job
Found something wrong with the page? Please let us know by submitting a report below.
Senior Clinical Trial Manager leading clinical trial delivery for ICON, a global healthcare intelligence and research organization. Overseeing start - up, execution, compliance, risks, budgets, and closeout.
Clinical Research Associate monitoring sponsor - dedicated clinical trials at ICON, the global clinical research organization. Ensuring protocol compliance, data integrity, and patient safety across trial sites.
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.
Clinical Research Associate monitoring clinical trials for ICON’s sponsor - dedicated research programs. Ensuring protocol compliance, data integrity, and patient safety across Canadian sites.
Senior Clinical Research Associate monitoring respiratory and cardiovascular trials for ICON in the Greater Toronto Area. Ensuring GCP compliance through site oversight, visits, data integrity, and stakeholder guidance.
Senior Clinical Research Associate monitoring respiratory and cardiovascular clinical trials for ICON in the Greater Toronto Area. Overseeing sites, compliance, data integrity, and trial execution.
Senior Clinical Scientist authoring clinical and regulatory documents for Indero, a global dermatology and rheumatology CRO. Supporting study design, data interpretation, submissions, and scientific teams.
Clinical Research Associate monitoring respiratory and cardiovascular trials for ICON Strategic Solutions in Canada's GTA. Managing site visits, compliance, data integrity, and CRA guidance.
Clinical Research Associate overseeing respiratory and cardiovascular clinical trials for ICON. Monitoring GTA sites, ensuring GCP compliance, and supporting trial execution.