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
- Solid 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.

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