Overview
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In this role you will oversee site management, clinical and central monitoring to safeguard patient safety, data integrity, and regulatory compliance. You will manage activities from activation to closeout, coordinate with cross-functional teams, and apply risk-based approaches to keep trials on track. You will engage with investigators and sites, support study budgets and timelines, and contribute to inspection readiness. This position offers remote work in the UK, Poland, Spain, or Bulgaria within a large, mission-driven organization.
Compensaciones / Ventajas
career development and progression
inclusive culture
supportive line management
technical and therapeutic area training
peer recognition
total rewards program
Responsabilidades
Oversee site management, monitoring and central monitoring deliverables with focus on patient safety and data integrity
Manage site interactions from activation through closeout, including recruitment and investigator payments as needed
Identify risks to delivery using operational data and escalate to project manager when necessary
Collaborate with Study Start Up, Patient Recruitment and Data Management to hit milestones (activation, enrollment, database lock)
Develop and maintain clinical study tools (e.g., Clinical Monitoring Plan)



and ensure CTMS and dashboards are usable
Coordinate training for study team on protocols, CRF completion, SOPs, data plans and timelines
Oversee resource allocations for CRAs and Central Monitors, monitor team conduct and risk to delivery
Review and provide feedback on functional plans and ensure quality of monitoring and site management deliverables
Interact with clients and cross-functional departments to report status and resolve protocol execution obstacles
Support inspection readiness and develop corrective action plans as needed
Provide performance feedback to line managers and support larger, more complex trials
Requisitos principales
Bachelor’s degree or RN xqbhyrx in a related field or equivalent combination of education, training and experience
Demonstrated ability to lead and align teams to milestones
Experience in international environments and in site management/monitoring
Knowledge of GCP/ICH guidelines and regulatory requirements
Strong communication, presentation and interpersonal skills
Good computer skills and familiarity with trial systems
Ability to apply risk management and problem solving to clinical trials
Moderate travel (~20%)
strong communication
conflict resolution
problem solving
CTMS
EDC
eDiary

Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

📌 Single Sponsor Global Clinical Trial Manager II (Solid CRA background) fully home based in UK, Polan (Santander)
🏢 Syneos Health
📍 Santander