Enhance clinical trial processes as an IWRS Monitor with Everest Clinical Research in Markham, Ontario. Engage in overnight support while ensuring accuracy in IWRS applications and client communications.

Everest Clinical Research is seeking a Clinical Trials IWRS Monitor to provide dedicated support on-site in Markham or remotely from anywhere in Canada. This full-time role involves coordinating user queries, monitoring data quality, and generating comprehensive documentation. You will collaborate with internal teams to ensure productive project execution and uphold high standards in clinical data management.

Key Responsibilities:
• Act as the primary contact for CTT users
• Support issue analysis and resolution with developers
• Monitor data accuracy and perform daily checks




• Coordinate database changes with proper documentation
• Generate and maintain CTT Requirements Specification documents

Requirements:
• Bachelor’s degree in health science or related field
• At least 3 years of clinical trial data experience
• Ability to work independently and communicate effectively
• Detail-oriented approach to data review
• Experience with CTT applications and user training

Utilize your expertise in data management to support Everest’s mission in clinical research excellence.
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📌 Clinical Trials IWRS Monitor in Ontario
🏢 Everest Clinical Research
📍 Ontario