Elevate your career with Everest Clinical Research as a Clinical Safety Data Associate. Contribute to safety data review for clinical trials in a dynamic and supportive environment, either on-site in Toronto or remotely across Canada.

Everest is looking for a detail-oriented Clinical Safety Data Associate. In this key position, you will ensure high-quality safety data management while collaborating closely with Project Managers and Clinical Data Managers. Ideal candidates will possess strong organizational skills and a broad knowledge base in clinical trial safety data coding and management.

Key Responsibilities:
• Develop standard safety data review plans and checklists
• Perform safety data review, identifying and resolving issues




• Coordinate high-quality data collection with project teams
• Provide medical advice during SAE reconciliations
• Conduct coding using MedDRA and WHODrug dictionaries

Requirements:
• RN, M.D., M.Sc., or Ph.D. in relevant fields
• 2-3 years’ experience in clinical trial data management
• Robust knowledge in safety data management
• Exceptional oral and written communication skills
• Ability to manage multiple projects effectively

Join Everest and play a crucial role in managing clinical safety data with a focus on quality and collaboration.
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📌 Clinical Safety Data Associate Everest (Ontario)
🏢 Everest Clinical Research Services
📍 Ontario