CRA II - Canada

Clinical Research Associates (CRA II – Senior CRA) – Canada I’m working with a leading mid sized CRO looking to hire experienced CRAs across multiple levels to support a growing clinical pipeline in Canada. What you’ll be doing: Managing site relationships and acting as the key point of contact Conducting monitoring visits (SIV, IMV, COV) across phases Ensuring ICH-GCP compliance and patient safety Supporting site performance, recruitment, and data quality Contributing to efficient study delivery and timelines What we’re looking for: CRA experience across II, III, or Senior level 2+ years independent monitoring experience Study exposure to Oncology, Cardiology, or Ophthalmology Strong knowledge of ICH-GCP and clinical trial processes Proven ability to manage sites and drive study delivery Fluent in French 💡 Opportunity to join a high-performing, globally recognised CRO with strong career development and project exposure. 📩 Interested or open to hearing more? Drop me a message.

The CRA II will manage site relationships and act as the key point of contact while conducting monitoring visits across various phases. They will ensure compliance with ICH-GCP and patient safety, support site performance, and contribute to efficient study delivery.

Candidates should have CRA experience at II, III, or Senior levels with at least 2 years of independent monitoring experience. A strong knowledge of ICH-GCP and clinical trial processes, along with proven site management skills, is required.

• Career development opportunities

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• CRA Experience
• Independent Monitoring
• Oncology
• Cardiology
• Ophthalmology
• ICH-GCP Compliance
• Patient Safety
• Site Management
• Study Delivery
• Data Quality
• Recruitment
• Monitoring Visits
• Study Exposure
• Fluent in French

Expérience minimale

2+ ans