Clinical Operations

• Oversee the operational conduct of clinical trials at contracted medical institutions within a defined country or region
• Provide leadership to Lead Site Coordinators and Site Coordinators as a subject matter expert and escalation point for operational issues
• Assess feasibility of research protocols by reviewing clinical, operational, and resource requirements and recommending suitable trials
• Monitor budget negotiations and study activation timelines to support timely site readiness
• Manage Study Coordinators and oversee the quality and results of their work through study reports, timesheets, site trackers, and other operational tools
• Drive process improvement and standardization of clinical trial operations in alignment with ICH GCP, regulatory requirements, and controlled documents
• Contribute to operational guidelines, templates, and procedures
• Create a work culture promoting process transparency, accountability, and continuous learning

Explore Operations Manager, Clinical Research at PSI CRO AG. Review requirements and application details.