Overview 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 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

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