Clinical Research Associate II — Medical Diagnostics (Ottawa)

Agilus Consulting Group; Ottawa; On-site; CAD 55,000 - 85,000; Full time

Job summary

Agilus by Synergie in Ottawa, Ontario is seeking a Clinical Research Associate II to support execution, monitoring, and regulatory compliance for medical device studies. You will coordinate with scientists, project managers, statisticians, and data managers while maintaining study documentation and TMFs in a fast-paced environment.

The ideal candidate holds a Science degree and 2+ years of clinical research or lab experience, with knowledge of GCP.

Qualifications

• Bachelor's degree in Science or equivalent experience.
• At least 2 years of clinical research or scientific laboratory experience.
• Veeva and TMF uploads are assets.
• Strong technical writing and documentation skills.
• Knowledge of Good Clinical Practice guidelines.

Responsibilities

• Prepare study-specific clinical research documentation.
• Maintain Trial Master Files with accuracy and compliance.
• Develop and update standard operating procedures.
• Coordinate logistics and operational support for clinical studies.
• Conduct remote monitoring activities to support study execution.
• Collaborate with scientists, project managers, statisticians, and data managers.
• Support the analysis and reporting of clinical study results.
• Ensure study activities comply with quality and regulatory requirements.

Skills

Strong technical writing

Attention to detail

Independent working

Team collaboration

GCP knowledge

Education

Bachelor's degree in Science or equivalent experience

Tools

Veeva

TMF uploads

Job description

Agilus by Synergie in Ottawa, Ontario is seeking a Clinical Research Associate II to support execution, monitoring, and regulatory compliance for medical device studies. You will coordinate with scientists, project managers, statisticians, and data managers while maintaining study documentation and TMFs in a fast-paced environment.

The ideal candidate holds a Science degree and 2+ years of clinical research or lab experience, with knowledge of GCP.