Join Everest Clinical Research as a Clinical Safety Data Associate, empowering clinical trials through skilled safety data management in Markham, Ontario, or remotely from Canada.

As a dedicated Clinical Safety Data Associate, you'll play a key role in managing safety data for clinical trials. This position requires a commitment to client service, along with expertise in medical coding and laboratory data management. You will develop review plans, coordinate with project teams, and ensure high-quality data through diligent review processes.

Key Responsibilities:
• Develop study safety data review plans and maintain checklists
• Perform safety data reviews according to established protocols
• Coordinate with Project Managers for quality data management




• Provide medical advice in reconciling safety events
• Assist in protocol reviews and ensure consistent laboratory data collection

Requirements:
• RN, M.D., or Ph.D. in health-related fields required
• 2-3 years of clinical trial data management experience
• Strong medical coding knowledge with relevant tools
• Excellent communication and organizational skills
• Ability to manage multiple projects independently

Leverage your clinical expertise in data safety and coding to support Everest’s cutting-edge clinical trials.
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