About this role
The Senior Clinical Trial Administrator is a key member of the Clinical Project Team, supporting the delivery of clinical research projects. This role focuses on coordinating study activities, maintaining high-quality documentation, and ensuring compliance with SOPs and regulatory requirements.
Full-time Temporary (6 months) Sponsor office-based
Key Responsibilities
• Coordinate and track study activities using project systems and tools, ensuring accurate and timely updates • Maintain Trial Master File (TMF) documentation, including quality control, audit readiness, and archiving activities • Support preparation of study and site materials in line with protocols, SOPs, and regulatory standards • Provide administrative and operational support to the project team, including meeting coordination, documentation, and communications • Liaise with internal teams, sites, and vendors to support study delivery, including shipment tracking and investigator meeting support Requirements
• Degree, diploma, or equivalent experience in clinical research or a related field • Experience in a clinical research or administrative role within a CRO or pharmaceutical environment • Strong organisational skills with attention to detail and ability to manage multiple tasks • Proficient in Microsoft Office tools (Word, Excel, PowerPoint) • Fluent English and Hebrew
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