Clinical Trials Associate

Job Summary

Supporting project delivery across multiple clinical trials, the full-time Clinical Trials Associate will coordinate documentation, maintain project portals, and ensure compliance while working remotely from the US or Canada.

Key responsibilities

• Coordinate and track system access for project team members to support efficient study execution
• Maintain project portals and perform quality checks to ensure documents are current, accurate, and version controlled
• Manage project documentation and ensure timely submission of records to the Trial Master File

Required qualifications

• Degree-level qualification or equivalent professional experience, plus at least one year of experience in a related role
• Proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint
• Knowledge of ICH, GCP, and applicable FDA or EU regulations
• Strong interpersonal skills with the ability to collaborate effectively across teams
• Proven ability to manage multiple priorities in a fast-paced environment