Clinical Trial Associate (Office-based)

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Clinical Trial Associate (Office-based)

Copenhagen

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The Clinical Trial Assistant plays a key role within Qmed Consulting to administer, maintain and coordinate the logistical aspects of clinical trials, while ensuring compliance with ISO standards, Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). The CTA also acts as a pivotal point of contact and support for the clinical trial team.

The CTA will be involved in most activities for the preparation of conducting and completing a Clinical Trial. You will be responsible for setting-up and maintaining the Trial Master Files (TMF), the Investigator Site File (ISF), and/or other electronic filing systems. You will prepare essential clinical trial documentation, distribute, track and file documents.

4 ratings

Published: 04-03-2021