Clinical Trials Associate
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Job Summary
Providing essential administrative and project tracking support, the full-time Clinical Trials Associate will ensure timely and accurate task completion for clinical project teams while working remotely across various locations in the US and Canada.
Key responsibilities
- Arrange and track system access for project team members, including Project Managers and CRAs
- Maintain and audit project documentation to ensure the latest revisions are available on project portals
- Assist with the preparation and shipment of clinical trial documentation, including the Investigator Site File
Required qualifications
- Degree level qualification or equivalent experience with a minimum of one year in a related role
- Proficiency in MS Office applications, including Outlook, Word, Excel, and PowerPoint
- Fluency in English and the language of the country of location
- Strong organizational skills and the ability to manage multiple tasks independently
- Demonstrated attention to detail and commitment to quality work
Complete Job Description
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