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
Robust 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.

📌 Bilingual Clinical Research Associate Quebec Quebec City
🏢 1001 Syneos Health
📍 Quebec City