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Job Description & How to Apply Below
Join Everest Clinical Research as a Clinical Research Assistant, providing remote options across Canada. Focus on medical writing, document management, and quality control in clinical research.
In this role, you’ll support Everest’s clinical research projects by overseeing quality control measures and ensuring the accuracy of important study documents. Your responsibilities include assisting in e-publishing and managing project timelines, showcasing your organizational skills. Engage with high-level professionals while enhancing your career in a respected CRO known for its commitment to quality.
Key Responsibilities:
• Provide support for medical writing and QC deliverables
• Verify and review clinical study protocols thoroughly
• Learn document e-publishing processes and standards
• Assist with documentation and archiving tasks
• Organize meetings and take minutes for DMC/DSMB
Requirements:
• Bachelor’s degree or higher in relevant fields
• Experience in clinical trials and data management
• Strong verbal and written communication skills
• Detail-focused with the ability to manage multiple tasks
• Team-oriented with excellent interpersonal skills
Bring your clinical research experience to Everest and contribute to meaningful healthcare advancements.
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