Clinical Trial Associate

An exciting opportunity has arisen for a Clinical Trial Associate to join a growing clinical operations function in Hertfordshire. This role is ideal for someone who thrives in a regulated environment, enjoys working with detail, and wants to build or strengthen a career in clinical trials administration and operations.

You will play a key role in supporting the smooth running of clinical studies by providing high‑quality administrative and operational support to Clinical, Regulatory and Pharmacovigilance (PV) teams.

The role Reporting into the clinical operations team, you will support multiple ongoing studies, contributing to compliance, quality and delivery across the clinical trial lifecycle.

Key responsibilities include:

Managing Trial Master File (TMF) activities, including set‑up, document filing, quality control checks and archiving of physical files
Supporting invoice management, including logging invoices, maintaining budget trackers and prep...