Clinical Research Associate

Clinical Research Associate to support Oncology studies and cover sites across the UK, performing site monitoring visits and managing project expectations and issues.

Requirements

• Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility to travel to sites as required