Elevate your career as a Clinical Research Safety Associate in Markham with Everest. Leverage your clinical research experience to ensure project compliance and support effective trial management.

In this role, you will serve as the DMC Secretary, managing administrative tasks and serving as the liaison between committees and sponsors. Key responsibilities include drafting committee charters, coordinating data reports, and supporting project management. Your two years of clinical research in pharmaceutical settings will be pivotal in carrying out this essential position.

Key Responsibilities:
• Serve as DMC Secretary for assigned projects
• Manage recruitment and engagement of committee members
• Draft and circulate committee charters for approvals
• Schedule and coordinate all committee meetings
• Perform quality control reviews on clinical documents

Requirements:
• M.Sc. or Ph.D. in a health-related field
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