Lead Clinical Research Associate Position Quebec

Overview

Elevate your career as a Lead Clinical Research Associate, focusing on site management in clinical studies. This role involves both in office and remote monitoring to ensure compliance and safety throughout the research process. We are seeking an experienced individual to oversee site qualification, site initiation, and interim monitoring. You will utilize your knowledge of ICH/GCP Guidelines and regulatory requirements to maintain data integrity while collaborating with site teams.

The responsibility also includes effective problem resolution and communication of responsible issues to the project team. Enhance your skills in clinical monitoring and ensure compliance in an agile research environment.

• Perform site initiation and close-out visits
• Evaluate site performance and communicate issues
• Conduct source document reviews and data verification
• Ensure the informed consent process is followed
• Manage project timelines and site-level activities

• Bachelor's degree in a related field
• Strong knowledge of GCP/ICH Guidelines
• Excellent computer and communication skills
• Up to 75% travel availability
• Experience mentoring junior CRAs