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Clinical Trial Associate - USA

Linical • Stuart, FL, US • published 2026-10-09 03:03:30.843189

Description

The Clinical Trial Associate (CTA) is responsible for the collection, review, tracking, maintenance and archiving of essential study documents in the Trial Master File (TMF), ensuring that project\- specific administrative documents are maintained, and sites are supplied with all required clinical materials and supplies. CTA reports to the Managers, Clinical Trial Associates (MCTA) in the Western Region. **Duties and Responsibilities** * Provides administrative support to the project team * Assists the Project Manager (PM) with written and verbal communications to the project team and sites * As required, assist in pre\-identifying sites * As required, assist in site feasibility including providing feedback regarding site responses to the project team and the Client * Collects (or assists with the collection of) initial essential documents from sites * As applicable, assist the study team in implementation activities including preparation, collection of Regulatory and Essential Documents, facilitation of IRB/IEC submission and approval process. Submits the study to the central IRB (if applicable, North America only) * Assists the PMs with the creation of study\-specific documents a...

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