Support clinical research projects at Worldwide Clinical Trials through document control, project tracking, and precise administrative coordination. Work across United States and Canada assignments.
As a Clinical Trials Associate, you provide administrative and project tracking support to clinical project teams. You help ensure assigned Project Delivery services tasks are completed accurately and on time. The work includes system access, clinical documentation, project information, and quality control.
Key Responsibilities: Arrange and track system access for project team members
Quality audit current document revisions on project portals
Prepare and ship clinical trial documentation




Maintain version control and submit documents to trial master file
Track project information and site medical question logs
Requirements: Degree qualification or equivalent experience
Minimum one year of related experience
Excellent written and verbal English
Robust organization, problem-solving, and attention to detail
Proficiency in Outlook, Word, Excel, and PowerPoint
Apply clinical documentation, quality control, and project tracking skills as a Clinical Trials Associate supporting Worldwide Clinical Trials.

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📌 Clinical Trial Associate Project Support (Quebec City)
🏢 Worldwide Clinical Trials
📍 Quebec City