Join Everest Clinical Research as a Clinical Safety Data Associate, focusing on safety data management. Enjoy flexible remote work opportunities or take part in our in office team in Toronto, Ontario.

This role is designed for a meticulous professional with a background in clinical trial data management. As a Clinical Safety Data Associate, you will be responsible for reviewing, coding, and managing safety data throughout the clinical trial process. Your expertise will ensure high-quality data and compliance with industry standards.

Key Responsibilities:
• Develop and maintain safety data review plans
• Review laboratory and safety data while documenting findings
• Collaborate with Clinical Data Managers for data accuracy




• Provide medical insights for SAE and coding activities
• Assess and confirm laboratory normal ranges and units

Requirements:
• Degree in Pharmacology or health-related sciences
• 2-3 years in clinical trial data management
• Familiarity with safety data coding practices
• Strong communication and organizational skills
• Independent with project management abilities

Be part of Everest's success in clinical research—support safety data processes with precision and excellence.
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📌 Everest Safety Data Associate Remote (Ontario)
🏢 Everest Clinical Research Services
📍 Ontario