Clinical Research Associate

Industry: Clinical Research / Life Sciences

Function: Clinical Operations / Research

About the Role

Seeking a Clinical Research Associate to support Oncology clinical trials across UK sites. The role involves independent site monitoring, study compliance, recruitment oversight and collaboration with clinical study teams.

Key Responsibilities

• Conduct site selection, initiation, monitoring and close-out visits in line with GCP.
• Support site recruitment plans and study delivery.
• Provide protocol and study training to assigned sites.
• Monitor site quality, protocol compliance and regulatory requirements.
• Track submissions, approvals, recruitment, CRF completion and data queries.
• Maintain TMF/ISF documentation and ensure accurate study records.
• Document monitoring findings, action plans and follow-up activities.
• Collaborate with study teams and site personnel to resolve issues.

Requirements

• Independent on-site monitoring experience within Oncology, particularly unblinded studies.
• Strong knowledge of GCP and ICH guidelines.
• Life science degree or equivalent clinical research industry experience.
• Willingness and flexibility to travel to UK study sites.

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