Randstad Professional, a leading HR services provider specializing in placing highly qualified professionals, is looking for a Clinical Study Administrator for our valued client in the Clinical R&D CSS division.
...As a Clinical Study Administrator, you will play a critical role within the clinical research team, providing administrative support and ensuring the timely and accurate management of essential study documents in compliance with regulations.
Key Responsibilities:
Building, maintaining, and managing the Trial Master File (v-TMF) and Clinical Trial Management System ((one)CTMS).
Creating and distributing regulatory binders and physical documents.
Supporting investigators and teams in resolving documentation and compliance-related issues.
Providing logistical support, including distribution of study materials and meeting organization.
Participating in process improvements related to (one)CTMS/v-TMF.
Assisting in the reporting and communication of clinical data.
Degree: Bachelor’s degree in a relevant field.
Experience: At least 1 year of experience in administrative support; clinical research experience is a plus.
Skills:
Strong organizational and communication abilities.
Attention to detail and the ability to manage multiple tasks.
Proficiency in Microsoft Office (Excel, Word, PowerPoint).
Languages: Excellent command of English; Dutch is a plus.
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