Clinical Research Associate

Clinical Research Associate will support Oncology studies and cover sites across the UK, performing site monitoring visits and working with sites to adapt, drive, and track subject recruitment plan in line with project needs.

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