Opportunity Description
Elevate your career in clinical research as a Clinical Trial Assistant with Everest Clinical Research in Markham, Ontario. This role involves liaising with sponsors, managing documentation, and supporting trial operations effectively.
You will be integral to ensuring compliance with ICH-GCP guidelines and local regulations. Collaborate with various stakeholders to compile essential documents, assist with regulatory submissions, and maintain trial master files. Your focus on detail and organization will support the successful operation of clinical trials in a dynamic environment.
Key Responsibilities:
• Interact with study sponsors and investigational sites
• Compile and review clinical site documentation
• Assist with regulatory document submissions
• Maintain and archive files in the TMF and CTMS
• Track monitoring plan compliance metrics
Requirements:
• Bachelor's degree in Life Sciences or related field
• Proven experience in administrative support
•...
You will be integral to ensuring compliance with ICH-GCP guidelines and local regulations. Collaborate with various stakeholders to compile essential documents, assist with regulatory submissions, and maintain trial master files. Your focus on detail and organization will support the successful operation of clinical trials in a dynamic environment.
Key Responsibilities:
• Interact with study sponsors and investigational sites
• Compile and review clinical site documentation
• Assist with regulatory document submissions
• Maintain and archive files in the TMF and CTMS
• Track monitoring plan compliance metrics
Requirements:
• Bachelor's degree in Life Sciences or related field
• Proven experience in administrative support
•...
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