Clinical Research Associate: Site Monitoring & Recruitment

IQVIA Inc; Kirkland; On-site; CAD 75,000 - 137,000; Full time

Benefits offered by this job

Health insurance

Job summary

IQVIA Inc. in Kirkland, Quebec, Canada is seeking a Clinical Research Associate to perform site monitoring and study management to ensure protocol compliance and data integrity.

This role includes monitoring visits, site training, and collaboration with study teams to support recruitment and regulatory submissions. The position requires a Bachelor's degree in a scientific discipline or healthcare, knowledge of GCP/ICH guidelines, and strong communication skills.

Qualifications

• Bachelor's degree in scientific discipline or health care preferred.
• Equivalent combination of education, training and experience may be accepted.
• Some organizations require CRA training or monitoring experience.
• Good knowledge of GCP and ICH guidelines.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope and regulatory requirements.
• Drive subject recruitment plans to enhance predictability.
• Administer protocol training and establish regular communication with sites.

Skills

GCP knowledge

ICH guidelines

MS Office

English communication

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA Inc. in Kirkland, Quebec, Canada is seeking a Clinical Research Associate to perform site monitoring and study management to ensure protocol compliance and data integrity.

This role includes monitoring visits, site training, and collaboration with study teams to support recruitment and regulatory submissions. The position requires a Bachelor's degree in a scientific discipline or healthcare, knowledge of GCP/ICH guidelines, and strong communication skills.