Clinical Research Associate II/III at Novotech
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Key Responsibilities
• Build relationships with site personnel for efficient 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. #J-18808-Ljbffr
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