We are seeking a Clinical Research Associate II to join a dynamic, multi-sponsor environment. This is an excellent opportunity for a motivated professional who thrives in a fast-paced setting, working across multiple protocols and clients, with a strong focus on oncology trials.

Key Responsibilities

• Independently perform on-site monitoring visits across the UK (site selection, initiation, monitoring, and close-out)
• Ensure clinical trials are conducted in compliance with ICH-GCP and applicable regulatory requirements
• Manage multiple studies and sponsors simultaneously, maintaining high-quality delivery
• Build and maintain strong relationships with investigators, site staff, and key stakeholders
• Identify and resolve site issues proactively to ensure timelines and data integrity are met
• Contribute to study documentation, reporting, and audit readiness

Essential Requirements