Lead clinical site oversight with ICH-GCP expertise at Novo in Greater Montreal Area, Quebec, traveling up to 70% of the time.

As a Senior Clinical Research Associate, you will manage assigned sites through secure, compliant, timely trial execution. Apply clinical trial methodology, regulatory requirements, and internal SOPs while partnering with investigators and site teams.

Your work supports reliable data, patient safety, and trial progress.

Key Responsibilities:

- Conduct on-site and remote monitoring visits
- Ensure compliance with protocols, ICH-GCP, and regulations
- Apply RBQM principles to identify and mitigate risks
- Track recruitment, retention, performance, and data collection
- Train site staff on protocols, systems, and compliance

Requirements:

- Bachelor's degree in Life Sciences or related field
- Five or more years of CRA experience
- Proficiency with EDC, CTMS, and eTMF systems
- Strong organizational, project management, and communication skills
- Ability to travel up to 70% of the time

Bring clinical monitoring, risk management, and patient safety expertise to Novo's assigned trial sites across Canada.

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📌 Senior Clinical Research Associate (Mississauga)
🏢 Novo
📍 Mississauga