Overview

The Senior CTA supports operational and development activities across assigned clinical studies. This role ensures efficient study execution, high-quality documentation, and effective oversight of CRO vendors and other operational partners. This is a long term contract role to be based in Basel (Hybrid).

Key Responsibilities

• Support study start-up activities, including collection and coordination of essential documents
• Contribute to site and vendor management activities
• Create, manage, and update trackers and logs to ensure oversight of trial progress
• Maintain a high-quality filing structure and oversee archiving of trial documentation
• Oversee and maintain the internal Trial Master File (TMF)
• Conduct regular oversight and quality checks of the external TMF

Qualifications

• Master’s degree required
• Experience supporting start-up and later-phase clinical trials
• Strong organizational, documentation, and communication skills
• Ability to collaborate cross-functionally and manage multiple priorities