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Expert Clinical Trial Documentation - Clinical Trial Associate (CTA)

Octapharma·Lachen·11.08.2026

 iventajobdata.eu

 
full_time80–100%

 

This Clinical Trial Associate role involves managing trial documents and supporting the clinical team. Daily tasks include setting up and maintaining files, tracking documents, and ensuring audit readiness. A minimum of 1 year of experience and fluency in English are required. Nice-to-have skills include German language proficiency and experience with CTMS and TMF systems. This role offers a chance to work on life-saving medicines and contribute to a great team. The company provides a market-related salary and benefits package.