Sr. CRA-Medical Device-Cardiology
On-site · Montréal, Quebec, Canada or Burlington, Ontario, Canada
Job Summary
Sr. CRA at ICON leads clinical trial monitoring across sites, ensuring adherence to study protocols, regulatory requirements, and GCP. Responsibilities include site visits, issue resolution, cross-functional collaboration, training site staff, and building strong relationships with site personnel and stakeholders to enable smooth trial operations. The role requires independent guidance of others, a strong foundation in monitoring processes, data integrity, and site management, and the ability to travel (~60%).
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate (CRA)
- Strong understanding of clinical trial processes and regulatory requirements
- Ability to manage multiple sites and projects independently
- Proficiency in monitoring practices, data integrity, and site management
- Proficiency with relevant clinical trial software and tools
- Excellent communication and stakeholder management skills
- Willingness to travel approximately 60%
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