Engage in impactful clinical research with Everest as a Clinical Research Safety Associate. Work from home in Canada or in the dynamic Markham office supporting crucial safety and data management tasks.

Everest Clinical Research is expanding its team and looking for a Clinical Research Safety Associate. In this vital role, you will coordinate with various stakeholders, manage documentation, and ensure that clinical trials meet regulatory standards. Your previous experience in the field will enhance your performance and contribute to project success.

Key Responsibilities:
• Act as DMC Secretary and oversee project administration
• Ensure all documents are compliant with regulatory standards
• Coordinate project activities with sponsors and teams




• Provide quality control on clinical research documentation
• Assist with medical writing and editing tasks

Requirements:
• M.Sc. or Ph.D. in a relevant discipline
• At least two years’ clinical research experience
• Familiarity with clinical trial regulations
• Solid organizational and detail-oriented skills
• Positive adaptability in team settings

Join Everest in delivering high-quality clinical research and making a genuine difference in patient safety.
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📌 Everest Clinical Research Safety Associate (Ontario)
🏢 Everest Clinical Research Services
📍 Ontario