May 17, 2026
Our client is a global pharmaceutical organisation conducting novel drug discovery & development projects across a broad range of therapeutic areas including Neuroscience, Inflammation, Immunology and Oncology etc.
In this role you will be supporting the delivery of clinical studies from protocol development through to final reporting and archiving. It’s a great opportunity for someone early in their clinical research career who enjoys organisation, collaboration, and continuous improvement.
Working closely with the Clinical Project Manager, you will help ensure studies run smoothly by coordinating plans, documentation, systems, and partners. You’ll play a central role in keeping teams aligned, maintaining high-quality records, and ensuring timelines and regulatory requirements are met.
Key responsibilities
* Maintain an accurate and audit-ready Trial Master File (TMF) through ongoing review and follow-up
* Support the preparation, review, and finalisation of key study...
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Unknown Status
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CV-Library
Slough, Berkshire
Contractor