Elevate clinical trials with Syneos Health as an Experienced Clinical Research Associate. Use your monitoring skills to ensure compliance and foster patient safety across multiple sites.

This role focuses on conducting essential site activities, including initiation, management, and close-out visits, with an emphasis on maintaining high standards of data integrity. You will actively assess site compliance with regulations and collaborate closely with study teams to overcome challenges. Your contributions will profoundly influence the advancement of therapies.

Key Responsibilities:
• Perform site initiation and monitoring visits
• Document site activities and compliance measures
• Review clinical data and address discrepancies




• Manage investigational product handling and logistics
• Facilitate training and compliance of site staff

Requirements:
• Bachelor’s degree or RN in a relevant field
• Familiarity with ICH-GCP Guidelines
• Proficiency in data management and analysis
• Exceptional communication and interpersonal abilities
• Regular travel requirements up to 75%

Utilize your skills and passion for research to drive excellence in clinical trials at Syneos Health.
J-18808-Ljbffr

📌 Experienced Clinical Monitor At Syneos Health Ontario (Canada)
🏢 Syneos Health
📍 Canada