Our client is a leading company in the Pharma Sector. We are seeking a Senior Clinical Research Associate to join our team Train and support investigator site teams on study procedures and systems Conduct site initiation, monitoring (on-site and remote), and close‑out visits Verify informed consent, study material management, and biological sample handling (if applicable) Monitor data accuracy and quality by verifying eCRF data against source documents Maintain investigator site files and manage essential regulatory documentation Provide technical support for eCRF systems and data entry Maintain regular communication with investigators and project teams Manage study archiving and support site billing processes If this is not possible, we search for a confirmed/senior CRA. Subject to the direction and coordination of Hays Plc