Lead high-quality clinical trials at Novo Nordisk as a Clinical Research Associate based in Montreal. Collaborate with stakeholders and ensure compliance for impactful patient outcomes.
In this role, you’ll oversee assigned trial sites, ensuring adherence to ICH-GCP guidelines and effective monitoring practices. A successful applicant should demonstrate strong project management capabilities, with a focus on relationship building and operational excellence throughout the trial process. This position also involves significant interaction with diverse teams.
Key Responsibilities:
• Conduct on-site and remote trial site monitoring
• Drive implementation of Risk-Based Quality Management
• Track site performance metrics and data integrity
• Mitigate risks by managing adverse events promptly
• Train site personnel on study operational protocols
Requirements:
• Bachelor’s degree in a relevant life sciences field
• 1+ years in clinical trial monitoring or CRO role...