Clinical Trials Associate

📋 Description

• Coordinate and track system access for clinical project team members, including Project Managers
• Maintain project portals and perform quality checks to ensure that the latest approved document
• Support the preparation, organization, and shipment of clinical trial documentation.
• Assist with the preparation and maintenance of Investigator Site Files (ISFs).
• Manage document version control and quality checks to ensure consistency and accuracy.
• Submit and maintain relevant documentation within the Trial Master File (TMF).

🎯 Requirements

• A university degree or equivalent professional experience.
• At least one year of experience in a related administrative, clinical research, or project support
• Excellent written and verbal English communication skills.
• Fluency in the language of the country where the candidate is based; for Canada, this means
• Strong organizational skills and the ability to manage multiple tasks simultaneously.
• Ability to exercise independent judgment and work with appropriate autonomy.

🎁 Benefits

• Remote working arrangement.
• Full-time position.
• Opportunity to contribute to clinical research projects with the potential to improve patient lives.
• Exposure to international clinical project teams and a collaborative global working environment.
• Salary range disclosed for the United States: USD 16.83–33.65 (the source does not specify whether
• A competitive benefits package is offered, with details depending on the employee’s location.