Senior Study Monitor

We're seeking a Senior Study Monitor to join our Field Clinical Trials team in France. The role involves conducting and overseeing monitoring activities across clinical trial sites, verifying data accuracy, and supporting the successful execution of clinical trials.

Requirements

• Conduct site monitoring activities for all phases of clinical trials
• Verify the accuracy, completeness, and quality of data collected at study sites
• Serve as the primary point of contact for assigned study sites and investigators
• Assist with the preparation and implementation of monitoring plans and study-related documentation
• Provide training to site staff on study protocols, GCP guidelines, and compliance requirements
• Compile detailed monitoring reports and communicate findings to the Clinical Trial Project Manager and other stakeholders
• Identify and escalate risks affecting study timelines, quality, or compliance, and recommend corrective actions
• Support the maintenance of study master files, ensuring organization and readiness for audits or submission
• Collaborate with team members to ensure smooth execution of monitoring activities and adherence to project timelines
• Promote adherence to organizational values and ethical research practices at study sites
• Provide guidance, technical support and training to Monitors, Assistant Monitors, Monitor Associates and peers where applicable