The Clinical Research Associate will support Oncology studies across the UK, performing

site monitoring visits including selection, initiation, monitoring, and close-out, in line with

Good Clinical Practice (GCP). They will

manage subject recruitment, provide protocol training, and establish communication with sites to ensure

project success. Responsibilities include

evaluating site practices, managing regulatory submissions, tracking enrollment, and maintaining study documentation such as

the Trial Master File and Investigator's Site File. The role involves

collaborating with the study team to support

project execution.

Qualified candidates should have

experience in independent on-site monitoring of

Oncology studies, strong knowledge of GCP and ICH guidelines, and a

life science degree or equivalent experience.

Flexibility to travel is required.