Clinical Research Associate - Central or East regions Germany

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Skills

GCP

Description

We are looking for a Clinical Research Associate to plan, execute and monitor clinical trials from site initiation through close-out.

You will ensure compliance with regulatory

requirements

, ICH-GCP and study protocols, while prioritising patient safety, data integrity and timelines.

As the primary link between the Project Manager, study sites and sponsor, you will have the opportunity to grow within our structured Professional Career Framework.

Key

Responsibilities

Site Feasibility & Selection…

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