Senior CRA - Canada

Job summary

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…

Job details

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.

What you’ll do

The Senior CRA 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.

Requirements

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 study exposure to Oncology, Cardiology, or Ophthalmology, is required.

Listed skills

• French · Preferred
• Recruitment · Preferred
• Organization · Preferred
• Attention to detail · Preferred
• Compliance · Preferred
• safety · Preferred
• Pipeline · Preferred
• Development · Preferred
• Google Cloud · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

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