The Clinical Research Associate will support Oncology studies and cover sites across the UK
Job Summary
The Clinical Research Associate will support Oncology studies and cover sites across the UK.
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
Matching Summary
The Clinical Research Associate will support Oncology studies and cover sites across the UK.
Skills & Requirements
Must-have
Oncology studies
Site monitoring visits
Subject recruitment plan
Protocol and study training
Quality and integrity evaluation
Trial Master File (TMF)
Nice-to-have
Career with greater purpose
Make an impact
Never stop learning
Key Requirements
Experience of independent on-site monitoring
In depth knowledge of GCP and ICH
Life science degree educated or equivalent industry experience