Job Description
Position: Clinical Trial Administrator/Clinical Study Coordinator
Location: Bedford, UK - On-site
Client: UK Clinical Research Company
Type: Permanent
Main Responsibilities
* Act as first point of contact for the clinical research unit, providing front-of-house support and ensuring smooth daily operations.
* Chase, collect and organise patient medical records, liaise with GP practices and physicians, and ensure all documentation is complete and compliant.
* Coordinate and schedule patient visits, maintaining accurate records and supporting participants throughout the study process.
* Provide administrative support across the site, including managing study files, tracking documentation, and assisting with regulatory or sponsor-related queries.
* Support clinical staff, research nurses, and study sponsors to ensure studies run efficiently and according to protocols.
Main Requirements
1. Experience in a clinical research site, GP surgery, hospital clinic, or similar healthcare setting (e.g., Coordinator, Administrator, Clinic Support, Medical Secretary, or Band 4 equivalent).
2. Strong organisational skills with the ability to chase information, manage records, prioritise tasks, ...