Clinical Research

• Plan and lead day-to-day activities for monitoring complex clinical studies
• Communicate project objectives, expectations, and status updates to clinical teams
• Take overall responsibility for country study commitments and timely, high-quality data delivery
• Provide project oversight and leadership for clinical deliverables
• Lead and manage clinical teams and relevant local and global staff
• Drive successful activation of trial sites
• Monitor clinical activity quality and address quality issues
• Review and approve site visit reports and ensure tracking, follow-up, and resolution of site issues
• Identify data-related issues and risks and develop contingency and mitigation plans
• Create and maintain project-specific plans, documents, and tools
• Support CRAs with site monitoring activities and provide solutions to site issues
• Oversee regulatory and in-house clinical staff to ensure required updates, reports, renewals, and end-of-study notifications comply with protocols, local regulations, ICH GCP, and governing procedures
• Coordinate training, processes, systems-related activities, and ad-hoc activities

Clinical Research jobs in Czechia

Local Clinical Study Manager – Eastern Europe