Take on an essential role as a Trial Master Files Specialist for clinical research studies in Canada. This remote position focuses on maintaining accurate documentation and TMF organization.
The Trial Master Files Representative collaborates with clinical research teams, project managers, and stakeholders to maintain essential study documentation. Your expertise will ensure TMFs are complete, well-structured, and compliant with regulations. This role thrives on attention to detail, effective communication, and the ability to manage multiple priorities within a fast-paced setting.
Key Responsibilities:
• Prepare and maintain TMFs for clinical studies
• Ensure documentation is accurate and accessible
• Review files for completeness and compliance
• Communicate with stakeholders to resolve issues
• Track missing or inconsistent documentation
Requirements:
• Bachelor’s degree in a relevant field
• Minimum 1 year of document management experience
• Strong skills in organization and detail orientation
• Proficiency in Microsoft Office applications
• Excellent communication and collaboration skills
This role is ideal for someone eager to deepen their expertise in clinical document management.
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