Elevate your career as a Clinical Research Associate II/III with Novotech, the leading full-service CRO. Focus on participant wellbeing and accurate trial data management to drive clinical success.

As a Clinical Research Associate at Novotech, you will be pivotal in site relationship management, ensuring clinical trials adhere to ICH GCP guidelines and regulatory standards. Your role will encompass building strong connections with Principal Investigators and coordinating with regulatory teams to support trial execution. You will also ensure participant recruitment and engagement while overseeing site monitoring and compliance throughout all clinical phases.

Key Responsibilities:
• Build relationships with site personnel for productive trial management




• Prepare site documents and support regulatory submissions
• Monitor investigational sites as per GCP guidelines
• Ensure timely reporting of trial data and participant safety
• Maintain the Trial Master File and clinical management systems

Requirements:
• Fluent in French
• Graduate in clinical or life sciences
• 1-2 years of CRA experience for CRA II
• 2-3 years for CRA III
• Strong time management and detail orientation

Become a part of the Novotech team, supporting clinical innovation and improving patient outcomes globally.
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📌 Clinical Research Associate II/III at Novotech (Ontario)
🏢 Life Sciences WA
📍 Ontario