Elevate clinical trials with Syneos Health as a Bilingual Clinical Research Associate in Quebec. Engage in vital site management, regulatory compliance, and patient safety while working from home.

In this role, you will perform site qualifications, monitoring, and management while ensuring strict adherence to ICH-GCP and company protocols. Collaborate with diverse teams in a fully integrated biopharmaceutical setting, enhancing patient care through effective communication and diligent oversight. Your expertise in clinical operations and bilingual capabilities will contribute significantly to achieving project objectives.

Key Responsibilities:
• Conduct site qualification, initiation, and monitoring visits
• Ensure regulatory compliance with ICH and GCP guidelines




• Verify informed consent processes for patient confidentiality
• Assess patient safety and data integrity at sites
• Document all activities according to SOPs and clinical plans

Requirements:
• Bilingual in French and English
• Experience in clinical monitoring and site management
• Knowledge of ICH/GCP guidelines
• Solid analytical and communication skills
• Comfortable with work from home dynamics

Utilize your clinical expertise and bilingual skills to make a difference in patients' lives with Syneos Health.
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📌 Bilingual Clinical Research Associate Quebec Quebec City (Canada)
🏢 1001 Syneos Health
📍 Canada