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 documentationOversee 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
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